This document provides 65 sample consulting niche opportunities for physicians to supplement their clinical income. Some key opportunities mentioned include becoming a physician consultant in areas like clinical trials, coding, compliance, expert witnessing, health informatics, and medical writing. As a consultant, physicians can be paid more fairly for their expertise while enjoying low overhead, intellectual challenge, and control over their work. Consulting allows physicians to transition out of clinical practice at their own pace.
The document summarizes a presentation on using big data to enable patient centricity in clinical research. It discusses how all players in healthcare are focusing on the patient and how pharma companies can overcome barriers to access patients. It also outlines different ways companies can understand and engage patients, including through interviews, online/mobile solutions, and financial support. The presentation notes that big data can provide a better understanding of healthcare consumers and ultimately enhance patient treatment across clinical trials and a drug's lifecycle. However, challenges around organizational culture, data governance, and technology adoption must be overcome to fully realize patient centricity.
Transforming Clinical Practice InitiativeCitiusTech
The Transforming Clinical Practice Initiative (TCPI) is designed to help small practices and clinicians achieve large-scale health transformation. The initiative is designed to support more than 140,000 clinician practices over four years duration in sharing, adapting and further developing their comprehensive quality improvement strategies. The TCPI is one part of a unique strategy advanced by the Affordable Care Act to strengthen the quality of patient care and manage health care expenditures, ultimately saving the taxpayer from substantial costs. This document describes the initiative in detail with the type of participants, eligibility and reporting requirements of the participants. Understanding the implementation of this initiative not only helps clinicians, but opens up a huge market for Healthcare IT companies offering the products and services like EHR implementation, Integration, EHR/ Data Migration, Implementation of HIE etc.
The State of Consumer Healthcare: A Study of Patient ExperienceProphet
Providers must deliver a holistic patient experience that extends beyond clinical care interactions. The current state of the patient experience is poor and getting worse according to surveys, with 81% of consumers unsatisfied. While providers see patient experience as important, they overestimate their performance by over 20 percentage points compared to consumer ratings. Improving patient experience can drive operational efficiencies and reduce costs while helping organizations achieve their missions. Providers must take a holistic view of patient experience, empower their staff, and thoughtfully invest in technologies to enhance the experience.
Ashfield Head of Clinical – Europe, Nagore Fernandez, presented at eyeforpharma 2017, sharing learnings from Ashfield’s 15 years of experience delivering patient support services. The presentation covers how to design, deliver and measure a truly differentiated patient support programme, as well as practical do’s and don’ts for success.
#e4pbarca #unitepharma, adherence, behaviour change, eyeforpharma 2017, patient enrolment, patient outcomes, patient support programmes, psp,
1) Retail clinics have experienced rapid growth in recent years, with the largest operators like MinuteClinic planning to open hundreds more clinics.
2) Major retail pharmacy chains like CVS and Walgreens have acquired the largest retail clinic operators to benefit from synergies with their retail businesses.
3) Surveys show that consumers are comfortable with and interested in using retail clinics for convenient, basic healthcare needs, demonstrating the potential for continued growth in retail clinics.
The document discusses blood bank accreditation. Accreditation is a voluntary process that assesses an organization's quality systems and commitment to continuous improvement. It focuses on learning, self-development, and reducing risks. Accreditation benefits users through improved safety and quality of blood services, and benefits blood banks by stimulating improvement, maximizing satisfaction, and raising community confidence. In India, the National Accreditation Board for Hospitals sets standards for blood bank accreditation.
The document discusses the role of Clinical Engineering Technologists at the Medical Equipment Service Unit (MESU) at Queen's Medical Centre NHS Trust in Nottingham. MESU employs 27 qualified Clinical Engineering Technologists who are responsible for managing over 20,000 medical devices valued at £25.5 million. The Technologists provide core services like medical device management, equipment library services, user training, and maintenance to ensure medical devices are functioning properly, used safely and effectively to support patient care. Some of the key work of Technologists includes evaluating new devices, managing devices throughout their lifecycle including safety testing, maintenance and repairs, incident investigations when devices malfunction, and calibration checks to ensure medical devices deliver accurate outputs and measurements.
The document summarizes a presentation on using big data to enable patient centricity in clinical research. It discusses how all players in healthcare are focusing on the patient and how pharma companies can overcome barriers to access patients. It also outlines different ways companies can understand and engage patients, including through interviews, online/mobile solutions, and financial support. The presentation notes that big data can provide a better understanding of healthcare consumers and ultimately enhance patient treatment across clinical trials and a drug's lifecycle. However, challenges around organizational culture, data governance, and technology adoption must be overcome to fully realize patient centricity.
Transforming Clinical Practice InitiativeCitiusTech
The Transforming Clinical Practice Initiative (TCPI) is designed to help small practices and clinicians achieve large-scale health transformation. The initiative is designed to support more than 140,000 clinician practices over four years duration in sharing, adapting and further developing their comprehensive quality improvement strategies. The TCPI is one part of a unique strategy advanced by the Affordable Care Act to strengthen the quality of patient care and manage health care expenditures, ultimately saving the taxpayer from substantial costs. This document describes the initiative in detail with the type of participants, eligibility and reporting requirements of the participants. Understanding the implementation of this initiative not only helps clinicians, but opens up a huge market for Healthcare IT companies offering the products and services like EHR implementation, Integration, EHR/ Data Migration, Implementation of HIE etc.
The State of Consumer Healthcare: A Study of Patient ExperienceProphet
Providers must deliver a holistic patient experience that extends beyond clinical care interactions. The current state of the patient experience is poor and getting worse according to surveys, with 81% of consumers unsatisfied. While providers see patient experience as important, they overestimate their performance by over 20 percentage points compared to consumer ratings. Improving patient experience can drive operational efficiencies and reduce costs while helping organizations achieve their missions. Providers must take a holistic view of patient experience, empower their staff, and thoughtfully invest in technologies to enhance the experience.
Ashfield Head of Clinical – Europe, Nagore Fernandez, presented at eyeforpharma 2017, sharing learnings from Ashfield’s 15 years of experience delivering patient support services. The presentation covers how to design, deliver and measure a truly differentiated patient support programme, as well as practical do’s and don’ts for success.
#e4pbarca #unitepharma, adherence, behaviour change, eyeforpharma 2017, patient enrolment, patient outcomes, patient support programmes, psp,
1) Retail clinics have experienced rapid growth in recent years, with the largest operators like MinuteClinic planning to open hundreds more clinics.
2) Major retail pharmacy chains like CVS and Walgreens have acquired the largest retail clinic operators to benefit from synergies with their retail businesses.
3) Surveys show that consumers are comfortable with and interested in using retail clinics for convenient, basic healthcare needs, demonstrating the potential for continued growth in retail clinics.
The document discusses blood bank accreditation. Accreditation is a voluntary process that assesses an organization's quality systems and commitment to continuous improvement. It focuses on learning, self-development, and reducing risks. Accreditation benefits users through improved safety and quality of blood services, and benefits blood banks by stimulating improvement, maximizing satisfaction, and raising community confidence. In India, the National Accreditation Board for Hospitals sets standards for blood bank accreditation.
The document discusses the role of Clinical Engineering Technologists at the Medical Equipment Service Unit (MESU) at Queen's Medical Centre NHS Trust in Nottingham. MESU employs 27 qualified Clinical Engineering Technologists who are responsible for managing over 20,000 medical devices valued at £25.5 million. The Technologists provide core services like medical device management, equipment library services, user training, and maintenance to ensure medical devices are functioning properly, used safely and effectively to support patient care. Some of the key work of Technologists includes evaluating new devices, managing devices throughout their lifecycle including safety testing, maintenance and repairs, incident investigations when devices malfunction, and calibration checks to ensure medical devices deliver accurate outputs and measurements.
The document discusses shortcomings of current clinical documentation improvement (CDI) programs and capabilities for more effective CDI. Some key shortcomings are that CDI programs are often reactive, focus only on increasing codes to boost reimbursement, do not consider long-term return on investment, and do not address the root cause of undercoding issues. More effective CDI should focus on proactively improving clinical documentation at its source to ensure accurate payment and minimize claim denials. This involves educating physicians on proper documentation practices rather than just querying cases after the fact. Advanced data analytics and tools to identify patterns of undercoding or overcoding can also help avoid denials.
How pharma and healthcare brands can improve their customer experienceJack Morton Worldwide
The SVP and Managing Director of Jack’s Chicago office, Matt Pensinger, presented at Lions Health 2015 with Katie Bang from Eli Lilly and Company about improving the customer experience for patients:
There is growing recognition amongst healthcare brands that understanding the full patient journey is essential for success in today’s healthcare environment. The sheer extent of this both physical and emotional journey, from awareness through to treatment and adherence, opens the patient to many potential experience gaps between their expectations and reality that can lead to frustration, disillusionment and even dropping the prescribed treatment.
So, healthcare companies must understand this journey if they are to improve the customer experience – and offer necessary patient support that extends far beyond a given medication. Being truly effective requires that the entire organisation (from science through to sales) understands the patient journey in order to meet patient needs and effectively engage the many stakeholders that are becoming increasingly important to a therapy’s success.
This is a significant undertaking and healthcare brands and their marketing agencies need to think differently about how they engage with patients and support communications for all the other stakeholders. This talk will examine the experience journey and what it means for the way we market.
Healthcare Delivery Reimagined: Patient Flow and Care Coordination AnalyticsAdrish Sannyasi
Come to learn how Splunk’s data analytics platform could be utilized to solve many high impact business problems in healthcare delivery systems to reduce cost, improve patient outcome and safety, and enhance care coordination experience. Analyze observed behavior from healthcare event data and metadata to discover patterns, monitor compliance, and optimize the workflow. Furthermore 80% of healthcare data is unstructured (clinical free text and documentation), or semi-structured and many new data sources are such as tele health, mobile health, sensors, and devices are getting integrated in many healthcare systems specifically in the area of chronic disease management. So, one need analytics software that can harvest, interpret, enrich, normalize, and model diverse structured and unstructured data and analytics approaches that embrace the “data turmoil” by relying less on standardized data items and more on the capability to process data in any format.
Use ACE Scores in Machine Learning to Predict Disease Earlier and Improve Out...Health Catalyst
The Adverse Childhood Experience (ACE) study conducted by the CDC and Kaiser Permanent showed a strong correlation between ACEs and negative health outcomes later in life (e.g., risky health behaviors, chronic health conditions, and early death). ACE scores help paint a more complete picture of a person’s health history—a more comprehensive data snapshot of the entire patient.
Given that ACE scores build better data sets and machine learning relies on high-quality data, health systems should incorporate these nutrient-rich data sources into their machine learning models to better predict negative health outcomes, allow for earlier interventions, and improve outcomes.
Healthcare machine learning is evolving to use ACE scores and lifestyle data (e.g., eating habits) to improve population health management.
Rodixon organiations study at polakkulathi narayanan renai medicityLibu Thomas
The document summarizes an organizational study conducted at Polakkulath Narayanan Renai Medicity hospital. The study aimed to understand the organization's different departments and their functions in a practical way beyond classroom knowledge. Key findings include that the hospital has experienced doctors and specialists across 36 departments but also faces tight competition. It was found that employees are mostly satisfied except regarding remuneration. The document also identifies strengths like modern facilities and opportunities in health tourism, as well as weaknesses like lack of employee input and threats from increasing competition in the growing healthcare industry.
Moving forward with the greater manchester formularyPM Society
The document discusses the development and implementation of a joint formulary across Greater Manchester to standardize prescribing and reduce unwarranted variation.
Some key points:
- The GM joint formulary aims to create consistency in prescribing across primary and secondary care within the region to improve patient care and reduce costs.
- Developing the formulary required significant consultation, leadership support, and governance structures to align 12 CCGs and providers.
- Implementation includes developing formulary chapters, monitoring use at practice level, and establishing a "do not prescribe" list to prevent postcode prescribing variation.
- Future plans include the formulary being maintained by the CSU, expanding monitoring capabilities, and developing partnerships with industry within ethical frameworks
This document summarizes a presentation on supply chain in the healthcare continuum. It discusses how the traditional healthcare model is shifting from acute care-focused to a new transformational model that supports various points of care across settings. This includes how facilities, talent, equipment, materials, revenue management, and information will need to adapt to this new model. It also discusses challenges like properly defining class of trade categories as care delivery moves outside hospitals. The presentation argues the supply chain will need new roles, players, and approaches to support the changing landscape of healthcare.
Patient experience has become increasingly important in healthcare. To improve patient experience, healthcare providers need to shift to a patient-centric model that focuses on all touchpoints of a patient's experience, from booking appointments to treatment and follow up. This requires training staff, enhancing technologies, personalizing care, and using data and feedback to continuously monitor and improve the patient experience.
Planning the implementation of an EMR or EHR, then you need to understand the basics of defining your clinical workflow. This presentation was made at a variety of medical conferences
This document summarizes an initiative by Duke Medicine's Private Diagnostic Clinic to improve patient access and appointment availability across several departments. It discusses:
1. FTI Consulting partnering with Duke to develop new governance structures and use analytics to increase appointments.
2. Two key elements of the project - a new appointment management framework and an "Access Algorithm" tool to measure and score access.
3. Recommendations to consolidate resources into a new "Access Practices Team" to oversee scheduling and hold departments accountable to access standards.
4. The "Access Algorithm" used 12 metrics like lag times, no-show rates, and utilization to score and compare access across specialties and identify areas for
How to Use Data to Improve Patient Safety: A Two-Part DiscussionHealth Catalyst
As healthcare organizations continue to experience expenses growing faster than revenues, value based care, and consumer transparency of costs and quality, patient safety will be an important determinant of success. This session will describe the sociotechnical attributes of a safe system, the challenges, the barriers and opportunities, and how to use data and your culture of safety as a powerful tool to drive down adverse events.
Attendees will learn:
Why patient safety and quality are important.
How data can help improve patient safety.
The history of patient safety and where we are today.
What components make up a safety analytics culture.
How the internal safety culture directly impacts patient safety metrics.
To describe basic guidelines for improving a safety culture with analytics.
A CEO's Keys to Continuous Quality ImprovementHealth Catalyst
The document discusses keys to continuous quality improvement at Thibodaux Regional Medical Center. It describes how the CEO Greg Stock engaged physicians by establishing a steering team led by physicians to drive care transformation. Analytics from their data warehouse and applications helped identify opportunities for improvement and support data-driven decisions. Driving organizational competence involved training staff on quality improvement methods and holding people accountable for ongoing monitoring of projects to ensure gains were maintained. Their sepsis improvement project alone saved 16 lives per year. The Joint Commission praised their methodology as a best practice for physician engagement and using data to drive improvement.
Clinical Integration: A Value-Based Model for Better CareHealth Catalyst
For many who work on the front lines of delivery system reform, clinical integration is not just a generic phrase to describe health care professionals working more closely together. It describes the enormous day-to-day efforts that allow hospitals and physicians to collaborate on improving quality and efficiency, while keeping the focus on clinical care and the patient.
Join Holly Rimmasch, Executive Vice President and Chief Clinical Officer at Health Catalyst, as she shares this framework and model for greater value care delivery.
Holly will discuss:
The key functions of a clinically integrated system
The key roles and processes critical to sustained improvement methodology
The importance of the organizational structure in supporting systemic improvement
We look forward to you joining us.
Presentation for spbt 2013 meeting background and researchklaffy
The document discusses the changing context of medical practice and the need for pharmaceutical representatives to build value-based relationships with physicians. It provides guidance on how representatives can validate their clinical knowledge through sub-specialty certification programs. The document also summarizes research that found physicians are more likely to meet with representatives who have completed specialized training programs developed by medical societies. Finally, it outlines the structure and attributes of an ideal disease-state training program for representatives.
Purpose of the Call:
•Review the results of the Canadian MedRec Audit Month
•Discuss lessons learned from the audit month – strengths and areas for improvement
•Suggest future value of audits and audit tools for your organization
•Gather ideas about how to improve the quality of MedRec at admission
Watch the recorded webinar: http://bit.ly/19aUYbU
"12 Steps to Better Healthcare" is filled with ideas that you can use right away to improve the efficiency and effectiveness of your healthcare organization. These steps can help you save time, money and lives, as you take part in the rebuilding of our healthcare system from the ground up.
Ambulatory Health Care Facility of the Future: Integrating Lean Workflow Rede...The Neenan Company
For more information, go to http://neenan.com or call 970.493.8747
As presented on March 19, 2010 at the 2010 AMGA Annual Conference
Presented by: Randall Huss, M.D., President, and Gerald Dowdy, VP Operations, St. John’s Clinic – Rolla Division; and Miguel Burbano de Lara, AIA, NCARB, Senior VP Healthcare, The Neenan Company
When faced with the opportunity of designing a new ambulatory facility to house a multi-specialty clinic practice, ASC and other outpatient services to be completed a year after implementation of their EHR, the St. John’s Clinic-Rolla team partnered with a progressive architectural team, The Neenan Company, to design and build a facility around the new electronic workflows. They integrated Lean workflow redesign and Lean facility design elements to achieve a facility capable of supporting the digital, paperless ambulatory practice of the future.
Purpose of the Call:
•Speakers from AHS will share:
•AHS’ approach to measurement for improvement (MedRec)
•Lessons learned throughout our measurement journey
•Their approach to using data to drive change at the frontline
The Medical Director oversees all activities of a company's Medical Department and contributes to senior leadership. Their day involves emails and phone calls about clinical trials, regulations, and health economics. They attend internal meetings on research, regulations, reimbursement, and business strategies. External meetings include advising investigators and regulators. As the senior medical advisor, they provide clinical guidance across the company.
Medical affairs department for small organizationDr. Zubair Ali
The document summarizes the drug development process and the role of medical affairs departments within pharmaceutical companies. It discusses the various phases of clinical drug trials from phase I to phase IV. It then outlines the structure and responsibilities of medical affairs, including clinical research, pharmacovigilance, medical information services, statistics management, and providing medical support to marketing and sales teams. A key part of medical affairs is the medical science liaison program which aims to educate medical professionals and support clinical trial recruitment through relationship building.
The document discusses shortcomings of current clinical documentation improvement (CDI) programs and capabilities for more effective CDI. Some key shortcomings are that CDI programs are often reactive, focus only on increasing codes to boost reimbursement, do not consider long-term return on investment, and do not address the root cause of undercoding issues. More effective CDI should focus on proactively improving clinical documentation at its source to ensure accurate payment and minimize claim denials. This involves educating physicians on proper documentation practices rather than just querying cases after the fact. Advanced data analytics and tools to identify patterns of undercoding or overcoding can also help avoid denials.
How pharma and healthcare brands can improve their customer experienceJack Morton Worldwide
The SVP and Managing Director of Jack’s Chicago office, Matt Pensinger, presented at Lions Health 2015 with Katie Bang from Eli Lilly and Company about improving the customer experience for patients:
There is growing recognition amongst healthcare brands that understanding the full patient journey is essential for success in today’s healthcare environment. The sheer extent of this both physical and emotional journey, from awareness through to treatment and adherence, opens the patient to many potential experience gaps between their expectations and reality that can lead to frustration, disillusionment and even dropping the prescribed treatment.
So, healthcare companies must understand this journey if they are to improve the customer experience – and offer necessary patient support that extends far beyond a given medication. Being truly effective requires that the entire organisation (from science through to sales) understands the patient journey in order to meet patient needs and effectively engage the many stakeholders that are becoming increasingly important to a therapy’s success.
This is a significant undertaking and healthcare brands and their marketing agencies need to think differently about how they engage with patients and support communications for all the other stakeholders. This talk will examine the experience journey and what it means for the way we market.
Healthcare Delivery Reimagined: Patient Flow and Care Coordination AnalyticsAdrish Sannyasi
Come to learn how Splunk’s data analytics platform could be utilized to solve many high impact business problems in healthcare delivery systems to reduce cost, improve patient outcome and safety, and enhance care coordination experience. Analyze observed behavior from healthcare event data and metadata to discover patterns, monitor compliance, and optimize the workflow. Furthermore 80% of healthcare data is unstructured (clinical free text and documentation), or semi-structured and many new data sources are such as tele health, mobile health, sensors, and devices are getting integrated in many healthcare systems specifically in the area of chronic disease management. So, one need analytics software that can harvest, interpret, enrich, normalize, and model diverse structured and unstructured data and analytics approaches that embrace the “data turmoil” by relying less on standardized data items and more on the capability to process data in any format.
Use ACE Scores in Machine Learning to Predict Disease Earlier and Improve Out...Health Catalyst
The Adverse Childhood Experience (ACE) study conducted by the CDC and Kaiser Permanent showed a strong correlation between ACEs and negative health outcomes later in life (e.g., risky health behaviors, chronic health conditions, and early death). ACE scores help paint a more complete picture of a person’s health history—a more comprehensive data snapshot of the entire patient.
Given that ACE scores build better data sets and machine learning relies on high-quality data, health systems should incorporate these nutrient-rich data sources into their machine learning models to better predict negative health outcomes, allow for earlier interventions, and improve outcomes.
Healthcare machine learning is evolving to use ACE scores and lifestyle data (e.g., eating habits) to improve population health management.
Rodixon organiations study at polakkulathi narayanan renai medicityLibu Thomas
The document summarizes an organizational study conducted at Polakkulath Narayanan Renai Medicity hospital. The study aimed to understand the organization's different departments and their functions in a practical way beyond classroom knowledge. Key findings include that the hospital has experienced doctors and specialists across 36 departments but also faces tight competition. It was found that employees are mostly satisfied except regarding remuneration. The document also identifies strengths like modern facilities and opportunities in health tourism, as well as weaknesses like lack of employee input and threats from increasing competition in the growing healthcare industry.
Moving forward with the greater manchester formularyPM Society
The document discusses the development and implementation of a joint formulary across Greater Manchester to standardize prescribing and reduce unwarranted variation.
Some key points:
- The GM joint formulary aims to create consistency in prescribing across primary and secondary care within the region to improve patient care and reduce costs.
- Developing the formulary required significant consultation, leadership support, and governance structures to align 12 CCGs and providers.
- Implementation includes developing formulary chapters, monitoring use at practice level, and establishing a "do not prescribe" list to prevent postcode prescribing variation.
- Future plans include the formulary being maintained by the CSU, expanding monitoring capabilities, and developing partnerships with industry within ethical frameworks
This document summarizes a presentation on supply chain in the healthcare continuum. It discusses how the traditional healthcare model is shifting from acute care-focused to a new transformational model that supports various points of care across settings. This includes how facilities, talent, equipment, materials, revenue management, and information will need to adapt to this new model. It also discusses challenges like properly defining class of trade categories as care delivery moves outside hospitals. The presentation argues the supply chain will need new roles, players, and approaches to support the changing landscape of healthcare.
Patient experience has become increasingly important in healthcare. To improve patient experience, healthcare providers need to shift to a patient-centric model that focuses on all touchpoints of a patient's experience, from booking appointments to treatment and follow up. This requires training staff, enhancing technologies, personalizing care, and using data and feedback to continuously monitor and improve the patient experience.
Planning the implementation of an EMR or EHR, then you need to understand the basics of defining your clinical workflow. This presentation was made at a variety of medical conferences
This document summarizes an initiative by Duke Medicine's Private Diagnostic Clinic to improve patient access and appointment availability across several departments. It discusses:
1. FTI Consulting partnering with Duke to develop new governance structures and use analytics to increase appointments.
2. Two key elements of the project - a new appointment management framework and an "Access Algorithm" tool to measure and score access.
3. Recommendations to consolidate resources into a new "Access Practices Team" to oversee scheduling and hold departments accountable to access standards.
4. The "Access Algorithm" used 12 metrics like lag times, no-show rates, and utilization to score and compare access across specialties and identify areas for
How to Use Data to Improve Patient Safety: A Two-Part DiscussionHealth Catalyst
As healthcare organizations continue to experience expenses growing faster than revenues, value based care, and consumer transparency of costs and quality, patient safety will be an important determinant of success. This session will describe the sociotechnical attributes of a safe system, the challenges, the barriers and opportunities, and how to use data and your culture of safety as a powerful tool to drive down adverse events.
Attendees will learn:
Why patient safety and quality are important.
How data can help improve patient safety.
The history of patient safety and where we are today.
What components make up a safety analytics culture.
How the internal safety culture directly impacts patient safety metrics.
To describe basic guidelines for improving a safety culture with analytics.
A CEO's Keys to Continuous Quality ImprovementHealth Catalyst
The document discusses keys to continuous quality improvement at Thibodaux Regional Medical Center. It describes how the CEO Greg Stock engaged physicians by establishing a steering team led by physicians to drive care transformation. Analytics from their data warehouse and applications helped identify opportunities for improvement and support data-driven decisions. Driving organizational competence involved training staff on quality improvement methods and holding people accountable for ongoing monitoring of projects to ensure gains were maintained. Their sepsis improvement project alone saved 16 lives per year. The Joint Commission praised their methodology as a best practice for physician engagement and using data to drive improvement.
Clinical Integration: A Value-Based Model for Better CareHealth Catalyst
For many who work on the front lines of delivery system reform, clinical integration is not just a generic phrase to describe health care professionals working more closely together. It describes the enormous day-to-day efforts that allow hospitals and physicians to collaborate on improving quality and efficiency, while keeping the focus on clinical care and the patient.
Join Holly Rimmasch, Executive Vice President and Chief Clinical Officer at Health Catalyst, as she shares this framework and model for greater value care delivery.
Holly will discuss:
The key functions of a clinically integrated system
The key roles and processes critical to sustained improvement methodology
The importance of the organizational structure in supporting systemic improvement
We look forward to you joining us.
Presentation for spbt 2013 meeting background and researchklaffy
The document discusses the changing context of medical practice and the need for pharmaceutical representatives to build value-based relationships with physicians. It provides guidance on how representatives can validate their clinical knowledge through sub-specialty certification programs. The document also summarizes research that found physicians are more likely to meet with representatives who have completed specialized training programs developed by medical societies. Finally, it outlines the structure and attributes of an ideal disease-state training program for representatives.
Purpose of the Call:
•Review the results of the Canadian MedRec Audit Month
•Discuss lessons learned from the audit month – strengths and areas for improvement
•Suggest future value of audits and audit tools for your organization
•Gather ideas about how to improve the quality of MedRec at admission
Watch the recorded webinar: http://bit.ly/19aUYbU
"12 Steps to Better Healthcare" is filled with ideas that you can use right away to improve the efficiency and effectiveness of your healthcare organization. These steps can help you save time, money and lives, as you take part in the rebuilding of our healthcare system from the ground up.
Ambulatory Health Care Facility of the Future: Integrating Lean Workflow Rede...The Neenan Company
For more information, go to http://neenan.com or call 970.493.8747
As presented on March 19, 2010 at the 2010 AMGA Annual Conference
Presented by: Randall Huss, M.D., President, and Gerald Dowdy, VP Operations, St. John’s Clinic – Rolla Division; and Miguel Burbano de Lara, AIA, NCARB, Senior VP Healthcare, The Neenan Company
When faced with the opportunity of designing a new ambulatory facility to house a multi-specialty clinic practice, ASC and other outpatient services to be completed a year after implementation of their EHR, the St. John’s Clinic-Rolla team partnered with a progressive architectural team, The Neenan Company, to design and build a facility around the new electronic workflows. They integrated Lean workflow redesign and Lean facility design elements to achieve a facility capable of supporting the digital, paperless ambulatory practice of the future.
Purpose of the Call:
•Speakers from AHS will share:
•AHS’ approach to measurement for improvement (MedRec)
•Lessons learned throughout our measurement journey
•Their approach to using data to drive change at the frontline
The Medical Director oversees all activities of a company's Medical Department and contributes to senior leadership. Their day involves emails and phone calls about clinical trials, regulations, and health economics. They attend internal meetings on research, regulations, reimbursement, and business strategies. External meetings include advising investigators and regulators. As the senior medical advisor, they provide clinical guidance across the company.
Medical affairs department for small organizationDr. Zubair Ali
The document summarizes the drug development process and the role of medical affairs departments within pharmaceutical companies. It discusses the various phases of clinical drug trials from phase I to phase IV. It then outlines the structure and responsibilities of medical affairs, including clinical research, pharmacovigilance, medical information services, statistics management, and providing medical support to marketing and sales teams. A key part of medical affairs is the medical science liaison program which aims to educate medical professionals and support clinical trial recruitment through relationship building.
This document summarizes a presentation given on rural health initiatives for primary care centers and eye care centers in East India. It discusses the Alchemist model of providing healthcare services to rural populations through a hybrid model of primary healthcare centers and eye care hospitals. Key aspects of the model include general medical care, diagnostic labs, pharmacies, eye refraction services, surgeries and outreach camps. 12 centers have been established across West Bengal, Bihar, Jharkhand and Odisha serving a population of 27 crore people. The workflow, infrastructure, outreach activities and expansion process are outlined. Examples of specific centers in Habra, Arrah and Chatra are also highlighted.
The Healthcare Revolution: 5 Ways a Consulting Firm Can Elevate Your PracticeAarohan healthcare
In today’s rapidly evolving healthcare landscape, staying ahead of the curve is essential for medical practices. Whether you run a small clinic or a large hospital, the challenges and opportunities presented by the healthcare revolution cannot be ignored. This article explores how consulting firms can play a pivotal role in elevating your practice to new heights.
The document provides advice for entry into the pharmaceutical and medical devices industry, including using recruitment agencies to find roles, preparing CVs and interview skills, and enhancing industry knowledge through experience, associations, conferences, and further education. It also outlines common entry-level positions and how to improve chances of securing a first role if initial applications are unsuccessful.
Educating KOLs, Physicians, Patients, and Payers to support successful produc...Best Practices, LLC
The document discusses best practices for educating key stakeholders to support successful product launches. It finds that companies should:
1) Start thought leader engagement early, as early as pre-clinical trials, through communication, advisory boards, and developing long-term strategies.
2) Seed medical science liaisons in phase 3 trials and grow their numbers each subsequent year leading up to launch.
3) Oncology companies may be more willing to take risks with investigator-initiated trials earlier to explore new uses and populations.
Delivering real world evidence to demonstrate product safety and valueKishan Patel, MBA
This document discusses how observational research and patient registries can provide real-world evidence on product safety and effectiveness. It outlines Quintiles' capabilities in this area, including experience conducting 195 patient registries and observational studies involving over 9 million patients. Quintiles claims it can help companies demonstrate products' performance in various populations and support regulatory and coverage decisions through generating real-world evidence.
Physicians undergo extensive education and training over approximately 25 years before practicing medicine. This includes medical school, residency, and potentially specialty training. However, doctors did not devote their lives to managing over 100 federal labor laws and regulations. Partnering with a professional employer organization (PEO) allows physicians to focus on patient care while the PEO handles HR-related responsibilities like payroll, benefits, and ensuring compliance. A PEO can provide services tailored to healthcare providers to help improve patient outcomes and support regulatory requirements.
Following our past four highly successful events, this event focuses on “A Critical Guide for Successfully Conducting “6th Annual Clinical Trials Summit 2015” It gives me great pleasure in welcoming all of you to The Virtue Insight’s “6th Annual Clinical Trials Summit 2015”.
Following our past four highly successful events, this event focuses on “A Critical Guide for Successfully Conducting “6th Annual Clinical Trials Summit 2015” It gives me great pleasure in welcoming all of you to The Virtue Insight’s “6th Annual Clinical Trials Summit 2015”.
The document discusses key strategies for hospital success, including establishing the business case for health information technology, redesigning processes around new technologies, and using technology to extend patient-centered care beyond hospital walls. It also covers best practices like incorporating evidence-based design principles in construction, including stakeholders in the design process, and designing flexibility into buildings. Additional topics include promoting economic viability, the benefits of electronic medical records, achieving patient-centered care, comprehensive care planning, and using social media and marketing.
Modern Healthcare 2014 Strategic Marketing Conference SlidesModern Healthcare
Thank you for joining us at the inaugural Strategic Marketing Conference, which took place Sept. 23 and 24 in Chicago. We hope you enjoyed the education, engaging in discussions and extending your professional networks.
Click here to view the program guide and agenda from the Strategic Marketing Conference:
http://www.modernhealthcare.com/assets/pdf/CH96416919.PDF
About the Conference:
Modern Healthcare's Strategic Marketing Conference is a two day educational conference that was held September 23 and 24, 2014 at the Hyatt Regency Chicago.
This year’s conference presented thought leaders in healthcare marketing who helped to guide healthcare marketers, focusing on consumer-driven, reform-led and economically necessary challenges. Modern Healthcare's Strategic Marketing Conference is an opportunity for healthcare marketing executives on the provider and supplier side to interact and collaborate on best practices. Throughout two days, the conference provides a unique opportunity for healthcare marketing executives and agencies representing providers, insurers, suppliers and advocacy groups to interact and collaborate on best practices.
Regulatory affairs professionals ensure public health by controlling the safety and efficacy of products. They keep track of changing legislation and advise their company on legal and scientific requirements. They collect and evaluate scientific data, present registration documents to regulatory agencies, and obtain marketing authorization for products. A good regulatory affairs professional helps maximize resources and serves as the first point of contact between a company and government authorities.
The Aequitas Group Capabilities Overview Q409bmeunier9
The Aequitas Group is a boutique strategic healthcare advisory firm that specializes in developing solutions to define and communicate a product's value. They deliver offerings in a disciplined, evidence-driven environment. Aequitas has experts from various healthcare fields and provides services across a product's lifecycle like clinical trials, market launch, reimbursement strategies, and more. Their goal is to maximize patient access through obtaining coverage, educating stakeholders, and navigating the regulatory landscape.
Nursing Peer Review to Improve Quality and Reduce Costs 2014iCareQuality.us
A system engineering approach is used to reduce frontline nursing care variability by integrating peer review to enhance quality of care efforts on the frontline.
5 Ways Healthcare Organizations Can Promote Patient SafetyAKW Medical
Patients and healthcare professionals can work together to improve patient safety to ensure a higher quality of care, reduce medical errors, and refocus on supporting good health and well-being.
Career In Clinical Research _ ProRelix Education (1).pdfTrishalaDeshmane1
Building a successful career in clinical research requires a strong foundation in science and medicine, specialized training in clinical research methodology, and a deep understanding of ethics and regulations
Overview of aspects of pharma's value added services and its primary aspects to deliver them.
Learn what others do and reflect how it's an opportunity for your pharma company..
As an owner and operator of urgent cares, Premier Health occupies a unique space because of it's joint venture business model. This electronic brochures gives readers insight into why Premier Health's motto "Your Business...Our Model" perfect describes what this company does and the competitive advantages for healthcare providers looking to get into urgent care.
Warhaftig Associates is an independent agency located in NYC that specializes in access, payer marketing, and patient support services for the pharmaceutical industry. They have 25 years of experience developing strategies and creative resources to help launch drug brands successfully and convey their value to key customers. Their full-service offerings include developing value propositions, patient support programs, appeals and reimbursement guidance, pull-through programs, and other specialized projects. They aim to understand customers' needs and help communicate a brand's unmet medical need, value, and budget impact through personalized engagements.
Similar to 6 proven-ways-to-supplement-your-clinical-income (20)
Gene therapy can be broadly defined as the transfer of genetic material to cure a disease or at least to improve the clinical status of a patient.
One of the basic concepts of gene therapy is to transform viruses into genetic shuttles, which will deliver the gene of interest into the target cells.
Safe methods have been devised to do this, using several viral and non-viral vectors.
In the future, this technique may allow doctors to treat a disorder by inserting a gene into a patient's cells instead of using drugs or surgery.
The biggest hurdle faced by medical research in gene therapy is the availability of effective gene-carrying vectors that meet all of the following criteria:
Protection of transgene or genetic cargo from degradative action of systemic and endonucleases,
Delivery of genetic material to the target site, i.e., either cell cytoplasm or nucleus,
Low potential of triggering unwanted immune responses or genotoxicity,
Economical and feasible availability for patients .
Viruses are naturally evolved vehicles that efficiently transfer their genes into host cells.
Choice of viral vector is dependent on gene transfer efficiency, capacity to carry foreign genes, toxicity, stability, immune responses towards viral antigens and potential viral recombination.
There are a wide variety of vectors used to deliver DNA or oligo nucleotides into mammalian cells, either in vitro or in vivo.
The most common vector system based on retroviruses, adenoviruses, herpes simplex viruses, adeno associated viruses.
This presentation gives information on the pharmacology of Prostaglandins, Thromboxanes and Leukotrienes i.e. Eicosanoids. Eicosanoids are signaling molecules derived from polyunsaturated fatty acids like arachidonic acid. They are involved in complex control over inflammation, immunity, and the central nervous system. Eicosanoids are synthesized through the enzymatic oxidation of fatty acids by cyclooxygenase and lipoxygenase enzymes. They have short half-lives and act locally through autocrine and paracrine signaling.
Storyboard on Acne-Innovative Learning-M. pharm. (2nd sem.) CosmeticsMuskanShingari
Acne is a common skin condition that occurs when hair follicles become clogged with oil and dead skin cells. It typically manifests as pimples, blackheads, or whiteheads, often on the face, chest, shoulders, or back. Acne can range from mild to severe and may cause emotional distress and scarring in some cases.
**Causes:**
1. **Excess Oil Production:** Hormonal changes during adolescence or certain times in adulthood can increase sebum (oil) production, leading to clogged pores.
2. **Clogged Pores:** When dead skin cells and oil block hair follicles, bacteria (usually Propionibacterium acnes) can thrive, causing inflammation and acne lesions.
3. **Hormonal Factors:** Fluctuations in hormone levels, such as during puberty, menstrual cycles, pregnancy, or certain medical conditions, can contribute to acne.
4. **Genetics:** A family history of acne can increase the likelihood of developing the condition.
**Types of Acne:**
- **Whiteheads:** Closed plugged pores.
- **Blackheads:** Open plugged pores with a dark surface.
- **Papules:** Small red, tender bumps.
- **Pustules:** Pimples with pus at their tips.
- **Nodules:** Large, solid, painful lumps beneath the surface.
- **Cysts:** Painful, pus-filled lumps beneath the surface that can cause scarring.
**Treatment:**
Treatment depends on the severity and type of acne but may include:
- **Topical Treatments:** Such as benzoyl peroxide, salicylic acid, or retinoids to reduce bacteria and unclog pores.
- **Oral Medications:** Antibiotics or oral contraceptives for hormonal acne.
- **Procedures:** Such as chemical peels, extraction of comedones, or light therapy for more severe cases.
**Prevention and Management:**
- **Cleanse:** Regularly wash skin with a gentle cleanser.
- **Moisturize:** Use non-comedogenic moisturizers to keep skin hydrated without clogging pores.
- **Avoid Irritants:** Such as harsh cosmetics or excessive scrubbing.
- **Sun Protection:** Use sunscreen to prevent exacerbation of acne scars and inflammation.
Acne treatment can take time, and consistency in skincare routines and treatments is crucial. Consulting a dermatologist can help tailor a treatment plan that suits individual needs and reduces the risk of scarring or long-term skin damage.
Spontaneous Bacterial Peritonitis - Pathogenesis , Clinical Features & Manage...Jim Jacob Roy
In this presentation , SBP ( spontaneous bacterial peritonitis ) , which is a common complication in patients with cirrhosis and ascites is described in detail.
The reference for this presentation is Sleisenger and Fordtran's Gastrointestinal and Liver Disease Textbook ( 11th edition ).
CLASSIFICATION OF H1 ANTIHISTAMINICS-
FIRST GENERATION ANTIHISTAMINICS-
1)HIGHLY SEDATIVE-DIPHENHYDRAMINE,DIMENHYDRINATE,PROMETHAZINE,HYDROXYZINE 2)MODERATELY SEDATIVE- PHENARIMINE,CYPROHEPTADINE, MECLIZINE,CINNARIZINE
3)MILD SEDATIVE-CHLORPHENIRAMINE,DEXCHLORPHENIRAMINE
TRIPROLIDINE,CLEMASTINE
SECOND GENERATION ANTIHISTAMINICS-FEXOFENADINE,
LORATADINE,DESLORATADINE,CETIRIZINE,LEVOCETIRIZINE,
AZELASTINE,MIZOLASTINE,EBASTINE,RUPATADINE. Mechanism of action of 2nd generation antihistaminics-
These drugs competitively antagonize actions of
histamine at the H1 receptors.
Pharmacological actions-
Antagonism of histamine-The H1 antagonists effectively block histamine induced bronchoconstriction, contraction of intestinal and other smooth muscle and triple response especially wheal, flare and itch. Constriction of larger blood vessel by histamine is also antagonized.
2) Antiallergic actions-Many manifestations of immediate hypersensitivity (type I reactions)are suppressed. Urticaria, itching and angioedema are well controlled.3) CNS action-The older antihistamines produce variable degree of CNS depression.But in case of 2nd gen antihistaminics there is less CNS depressant property as these cross BBB to significantly lesser extent.
4) Anticholinergic action- many H1 blockers
in addition antagonize muscarinic actions of ACh. BUT IN 2ND gen histaminics there is Higher H1 selectivitiy : no anticholinergic side effects
STUDIES IN SUPPORT OF SPECIAL POPULATIONS: GERIATRICS E7shruti jagirdar
Unit 4: MRA 103T Regulatory affairs
This guideline is directed principally toward new Molecular Entities that are
likely to have significant use in the elderly, either because the disease intended
to be treated is characteristically a disease of aging ( e.g., Alzheimer's disease) or
because the population to be treated is known to include substantial numbers of
geriatric patients (e.g., hypertension).
Can Traditional Chinese Medicine Treat Blocked Fallopian Tubes.pptxFFragrant
There are many traditional Chinese medicine therapies to treat blocked fallopian tubes. And herbal medicine Fuyan Pill is one of the more effective choices.
The biomechanics of running involves the study of the mechanical principles underlying running movements. It includes the analysis of the running gait cycle, which consists of the stance phase (foot contact to push-off) and the swing phase (foot lift-off to next contact). Key aspects include kinematics (joint angles and movements, stride length and frequency) and kinetics (forces involved in running, including ground reaction and muscle forces). Understanding these factors helps in improving running performance, optimizing technique, and preventing injuries.
Giloy in Ayurveda - Classical Categorization and SynonymsPlanet Ayurveda
Giloy, also known as Guduchi or Amrita in classical Ayurvedic texts, is a revered herb renowned for its myriad health benefits. It is categorized as a Rasayana, meaning it has rejuvenating properties that enhance vitality and longevity. Giloy is celebrated for its ability to boost the immune system, detoxify the body, and promote overall wellness. Its anti-inflammatory, antipyretic, and antioxidant properties make it a staple in managing conditions like fever, diabetes, and stress. The versatility and efficacy of Giloy in supporting health naturally highlight its importance in Ayurveda. At Planet Ayurveda, we provide a comprehensive range of health services and 100% herbal supplements that harness the power of natural ingredients like Giloy. Our products are globally available and affordable, ensuring that everyone can benefit from the ancient wisdom of Ayurveda. If you or your loved ones are dealing with health issues, contact Planet Ayurveda at 01725214040 to book an online video consultation with our professional doctors. Let us help you achieve optimal health and wellness naturally.
Nano-gold for Cancer Therapy chemistry investigatory projectSIVAVINAYAKPK
chemistry investigatory project
The development of nanogold-based cancer therapy could revolutionize oncology by providing a more targeted, less invasive treatment option. This project contributes to the growing body of research aimed at harnessing nanotechnology for medical applications, paving the way for future clinical trials and potential commercial applications.
Cancer remains one of the leading causes of death worldwide, prompting the need for innovative treatment methods. Nanotechnology offers promising new approaches, including the use of gold nanoparticles (nanogold) for targeted cancer therapy. Nanogold particles possess unique physical and chemical properties that make them suitable for drug delivery, imaging, and photothermal therapy.
TEST BANK For Brunner and Suddarth's Textbook of Medical-Surgical Nursing, 14...Donc Test
TEST BANK For Brunner and Suddarth's Textbook of Medical-Surgical Nursing, 14th Edition (Hinkle, 2017) Verified Chapter's 1 - 73 Complete.pdf
TEST BANK For Brunner and Suddarth's Textbook of Medical-Surgical Nursing, 14th Edition (Hinkle, 2017) Verified Chapter's 1 - 73 Complete.pdf
TEST BANK For Brunner and Suddarth's Textbook of Medical-Surgical Nursing, 14th Edition (Hinkle, 2017) Verified Chapter's 1 - 73 Complete.pdf
The Children are very vulnerable to get affected with respiratory disease.
In our country, the respiratory Disease conditions are consider as major cause for mortality and Morbidity in Child.
Selective alpha1 blockers are Prazosin, Terazosin, Doxazosin, Tamsulosin and Silodosin majorly used to treat BPH, also hypertension, PTSD, Raynaud's phenomenon, CHF
Computer in pharmaceutical research and development-Mpharm(Pharmaceutics)MuskanShingari
Statistics- Statistics is the science of collecting, organizing, presenting, analyzing and interpreting numerical data to assist in making more effective decisions.
A statistics is a measure which is used to estimate the population parameter
Parameters-It is used to describe the properties of an entire population.
Examples-Measures of central tendency Dispersion, Variance, Standard Deviation (SD), Absolute Error, Mean Absolute Error (MAE), Eigen Value
Discover the benefits of homeopathic medicine for irregular periods with our guide on 5 common remedies. Learn how these natural treatments can help regulate menstrual cycles and improve overall menstrual health.
Visit Us: https://drdeepikashomeopathy.com/service/irregular-periods-treatment/
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4. Ambulatory Surgery Centers: Work with clients with strategy development, marketing,
implementation, financial planning, patient satisfaction, and performance.
5. Biopharmaceutical: Assist with providing strategic, technical, and regulatory solutions for
biopharmaceutical product development.
6. Bundled Care: Work with clients to assess, design, and implement bundled payments,
reducing inefficiencies and costs, and negotiate fair compensation.
7. Business Consulting: Work with startups to help bring new invention, products, and
services to market.
8. Capital Budgeting and Planning: Assist in compiling facility condition data, cost-effective
deferral maintenance plans, capital planning measure and maximize capital assist ROI.
9. Care Delivery and Management: Assist healthcare companies, reduce costs and complexity
of operating systems, and deliver better value for patients.
10. Career Coaching: Assist other physicians in career choices, selection, transitions,
improvement, and development.
11. Case Management: Perform early intervention assessment, life care planning, catastrophic
case management, and evaluation.
12. Clinical Development: Work with clients to achieve effective delivery of clinical operation
services, including: physician advisor role implementation, operational and clinical process
redesign, and practice development.
13. Clinical Documentation: Assist physicians and medical groups with improving clinical
documentation to identify diagnosis, comorbidities, mitigate medical necessity, and receive
credit for complexity of their patient population.
14. Clinical Integration: Work with health care providers to coordinate and integrate the
clinical care to patients. Assist with value-based competition.
15. Clinical Trials: Assist with the design and execution of study protocols (Phase I-IV), case
and study reports, informed consent, and surveillance trials.
16. Coding: Work with physician offices, group practices, clinics, or specialty centers to assign,
review, and assure compliance with CPT, ICD-9CM, and HCPCS.
17. Compliance: Assist with audits of billing and compensation to assure Medicare and IRS
compliance.
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18. Continuity of Care: Assist providers to help them improve communication systems between
primary care physicians and consultants to avoid disruption in care, delayed diagnosis,
unnecessary testing and iatrogenic complications.
19. Contracting: Assist physician practices with manage healthcare contracting.
20. Cost Reduction: Work with physician practices to reduce administrative costs in billing and
reimbursements programs.
21. Credentialing: Assisting with initial credentialing, re-credentialing, credentialing reviews,
and hospital privileges.
22. Denial Management: Assist providers with their Medicare, Medicaid, and managed care
denials. Work to improve pre-admission documentation, eligibility process, and evaluate
Local Coverage Determinations, LCD's to avoid denials.
23. Disease Management: Assist with disease management (DM) to encourage proactive
treatment of acute and chronic conditions. Use of predictive modeling, identification, and
prevention of unnecessary emergency room visits and admissions.
24. Due Diligence: Assist venture capital and other groups to help assess the financial viability
and potential of products, companies, and acquisitions.
25. Disability Consulting: Work with insurers, IROs, TPAs, etc. to perform short-term and
long-term disability assessment. Physicians read and analyze medical and other records and
write reports answering the questions posed by client.
26. E Visits: Work with providers to develop the ability to respond or interact with patients
through a secure electronic channel. Assure compliance with HIPAA regulations.
27. Expert Witnessing: Work with attorneys and insurers in reviewing records, writing reports,
and testifying at depositions and trials in personal injury, malpractice, product liability, and
other litigation matters.
28. Fair Market Value (FMV) Opinions: Assist physicians and health systems with service
arrangements for buy-sell transactions, joint venture transactions, and mergers and
acquisitions.
29. Health Enterprise: Assist in creating a healthy environment for employees, reduce absence
related costs, and engaging employees to improve retention and productivity.
30. HIPAA: Assist with HIPAA compliance including risk assessment, training, disclosure
assessment, and audits.
31. Human Resources: Assists HR with physician/staff relations, retention, wellness, diversity,
and compliance.
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32. IMEs: Perform independent medical examinations of workers injured in industrial accidents,
personal injuries, or other matters in litigation. Physicians write reports and may testify at
depositions, hearings, or trials.
33. Informatics: Work with physicians, groups, hospitals to achieve the effective management
of computer technology for patient care research and education. Assist with the evaluation,
integration, and implementation of EHR compliance and adoption by physicians.
34. Integrated Care Management: Work with employers to prevent/control chronic medical
conditions to help control and reduce medical costs, admission, and re-admission rates. Use
health promotion, early detection, and appropriate management of existing diseases and
complications to mitigate chronic disease costs.
35. Leadership Development: Assist physician practices giving them the tools and resources to
manage effectively.
36. Long-term Care Facilities: Work with long-term and assisted living facilities to assist with
reimbursements, billing, clinical, and operational functions.
37. Marketing: Assist with market research for pharmaceutical markets, developing product
information, competitive product literature, and key opinion intelligence. Work with CME,
sales force training, and informational brochures for patients.
38. Medical Affairs Consulting: Work with pharmaceutical companies to provide scientific
support for late stage development and post market support for drugs and devices. Act as
disease experts, review documents for accuracy for regulatory review, and assist with
thought leader development.
39. Medical Devices: Work with companies for market assessment, product development,
commercialization, reimbursement, and market access.
40. Medical Writing: Assist companies and organizations with regulatory writing (for approval
of drugs, devices, and biologic) common technical documents, education writing for
physicians (CME), marketing materials, journalism, manuscripts, case reports, abstracts,
posters, brochures, slide decks, and journal articles.
41. Medicare Compliance: Work with providers to improve their compliance with Medicare
statutes and improve reimbursement.
42. Online Member Portals: Work with providers to customize member health portals to assist
TPA's and administrators. Assist with eligibility, claims, notifications, authorizations, and
integration.
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43. Patient Access: Assist with providers to establish and maintain adequate patient access
procedures. Work on issues such as: patient scheduling, insurance verification, pre-
registration and emergency and outpatient registration.
44. Patient Safety: Work with providers to achieve a culture of safety and clinical quality
improvement using evidence based medicine adherence.
45. Payer Analytics and Reporting: Assist providers with health analytics, discovering drives
of high cost of services, PPS payment, cost of referrals, and physician scoring.
46. Pharmacovigilance: Assist with drug safety with the collection, detection, assessment,
monitoring, and prevention of adverse effects with pharmaceutical products both pre and
post marketing.
47. Physician Benefit Management: Work with providers to optimize pharmacy benefit
management leverage, vendor relationships, use of physician administered medications, and
assist in achieving cost savings.
48. Physician Collaborative: Assist medical device and pharmaceutical companies to assure
compliance when contracting with and compensating physicians. Work to avoid conflicts of
interests and stay within industry norms and guidelines.
49. Physician Compensation: Work with physicians to assist them with Stark Law and anti-
kickback compliance.
50. Physician Documentation: Work with physicians and providers to empower physicians
with the tools and motivation to improve physician documentation.
51. Physician Hospital Relations: Work with physicians and hospitals to improve collaboration,
improve retention, physician satisfaction, and improve clinical and financial outcomes.
52. Population Health: Assist with support for health care management in planning, building,
and operating population health management functions.
53. Practice Development: Work with physician practices to achieve excellent patient outcomes
and satisfaction, practice growth, and increased profitability.
54. Procurement: Work with providers to assist in achieving operational efficiencies, strategic
sourcing, and reduction of procurement costs.
55. Publication Planning: Assist with biomedical publication in support of pharmaceutical
products with scientifically based submissions and compliance with ethical standards.
56. RAC and External Audits: Assist physician group prepare for Medicare Recovery Audits.
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57. Revenue Cycle Management: Assist in identifying opportunities to accelerate cash flow
with improved receivable management.
58. Risk Management: Assist physicians and facilities with efforts to reduce liability exposure
when practicing medicine. Make recommendations on: Patient confidentiality, failing office
equipment, medication samples, after hour phone calls from patients, critical test results,
communication with patients, use of chaperones, and dealing with patient complaints.
59. Startup Guidance: Work with physicians starting a practice to assist with planning, site
selection, governance, equipment acquisition, policies, and procedures, credentialing, and
marketing.
60. Surgery Center: Assist surgery centers, hospital operating rooms with analysis, redesign,
planning implementation
61. Telemedicine: Assist with program design, strategic planning, orientation, operational
policies and procedures. Work to assist in recruiting, credentialing, training, evaluation, and
marketing programs.
62. Think Tanks: Work with consulting research and advisory services companies on issues
such as business affairs, academic medical center issues, healthcare information technology,
and organizations design and development.
63. Total Population Health Management: Assist providers with comprehensive care and
management of total cost risk including evidence based clinical decision making, patient
engagement, and community integration.
64. Utilization Reviews: Assist insurers and IROs by reviewing medical records and reporting
on authorization of medical care. Includes precertification reviews and retrospective reviews.
65. Workflow Solutions: Assist medical practices to help integrate their workflow areas to
achieve maximum efficiency. Work in areas such as operations management, medical
records, and clinical area patient flow.
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Get a patent: Under the new patent statute first to file is the law of the land.
Get a patent attorney or patent agent to assist you getting started with a provisional patent
application.
Consider licensing your invention instead of trying to build your own company.
Have realistic expectations as companies prefer to buy into your idea and invention when
they can provide smaller upfront payments and a reasonable royalty.
Royalties for inventions can range from 3% to 7% of sales.
Develop a Business Plan for Your Invention
The plan should be detailed and thoroughly researched.
Address market size, potential revenue, compensation, and what your invention brings to the
table.
Develop a Prototype
To successfully approach companies about licensing your invention you ideally will have a working
prototype to show them. There are many companies which, for a fee, will help you build a prototype.
Get a Good Patent Attorney
Obtain an experienced patent attorney with a track record of success as early on in the process as
possible. Counsel will be able to guide you through the process, help you avoid the pitfalls, and
protect your invention by negotiating an airtight license and contract.
Conclusion
Physicians who want to succeed as an inventor need to be prepared to work hard, obtain the
necessary help, and treat inventing as a business as opposed to a hobby.
To help physicians get started on the road to success as a physician inventor, SEAK has developed a
training course: How to Become a Successful Physician Inventor: Bringing Your Ideas to Market.
For additional information about the course, visit: www.SupplementalIncomeForPhysicians.com
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A lot. One of the nation’s leading IME experts, based on extensive research, estimates that the
overall market size is between $3.5 and $4.0 billion annually. At $830 on average for a routine
IME, that translates into roughly 450,000 IMEs performed annually.
5. What specialties have the greatest opportunity to perform IMEs?
The specialists that perform the vast majority of IMEs are physiatrists, psychiatrists,
psychologists, neurologists, neurosurgeons, orthopedists, specialists in pain medicine,
chiropractors, and occupational medicine physicians. However, there is work available for just
about any specialty, depending on the nature of the injury or illness claimed.
6. How do I get trained to perform IMEs?
The following national organizations offer training for IMEs:
The American Board of Independent Medical Examiners (ABIME) (www.abime.org)
The American Academy of Disability Evaluating Physicians (AADEP)
(www.aadep.org)
The American College of Occupational and Environmental Medicine (ACOEM)
(www.acoem.org)
SEAK, Inc. (www.seak.com)
7. What are clients typically looking for when selecting an IME physician?
The clients look for:
A physician still treating patients, sometimes called "active practice"
Availability
Board certification
Careful review of the medical records
Effectiveness in writing reports and in testifying
Excellent reputation
Impartiality
Reasonable cost
Timely responsiveness
8. How much can I charge for each exam?
It depends. Many states’ workers’ compensation systems have fee schedules which dictate how
much independent medical examiners may charge. Generally in the tort system there is no hard
rule on how much you can bill. The fees are controlled by market forces including the
complexity of the case, the amount of money at stake, your skills, and your reputation.
Whatever you charge for an IME should be the full amount you collect unlike Medicare and
HMOs.
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SEAK conducted a national survey of IME fees in 2007 and found that the average amount
charged for a brief IME was $597, the average amount charged for a routine IME was $830 and
the average amount charged for a complex IME was $1,325. The full results of the survey are
available for sale on www.seak.com. Tort IMEs on average were found to be significantly more
lucrative for the examiner than workers’ compensation IMEs.
9. How much money can I expect to make?
There are numerous IME doctors who are substantially retired from clinical medicine, do IMEs
one or two days a week, and make a six figure income. Other doctors perform IMEs one day a
week while practicing clinical medicine and generate an additional six figure income. Some
doctors perform IMEs full time and make as much or more than practicing surgeons.
IME practices typically also generate supplemental income. A percentage of cases will lead to
depositions, court testimony, peer and disability reviews. Physicians routinely charge at least
$500/hour or more for their time associated with expert testimony, so this aspect of IMEs
enhances earnings. IME physicians also routinely charge for no-shows, meaning they often get
paid even if the examinee doesn’t show up. According to SEAK’s 2007 Survey of IME Fees
and Billing Procedures, the average no-show fee was $320.
10. How do I get referrals?
Perhaps the easiest way to get started doing IMEs is to list yourself with one or more IME
Brokers or companies or referral services. These firms provide IMEs for employers, insurers,
claims managers, third party administrators, employers and attorneys. The IME industry is
greatly fragmented and there may be numerous IME brokers or referral organizations operating
in your geographic location.
For workers’ compensation IMEs, many states maintain lists of examiners who are approved to
do workers compensation IMEs. Contact your state’s workers’ compensation agency and get
yourself placed on the list.
Directly contact local defense firms, insurance companies, employers and third party
administrators and let them know you are available for this work. To find defense firms, try the
legal reference Martindale Hubbell, which can be found in most public libraries and online at
www.martindale.com . You’d be looking for insurance defense, personal injury defense, and
workers’ compensation defense firms and lawyers. At insurance companies and third party
administrators the claims adjuster or case manager is the person who most frequently orders
IMEs. To find the larger insurance companies, case managers, claims adjusters and third party
administrators one resource you can use is the Business Insurance Market SourceBook, which is
published annually by Business Insurance. For employers, check with the largest employers in
your area. Very large employers are often self-insured.
List yourself in SEAK’s National Directory of Independent Medical Examiners
(www.imedirectory.com). SEAK’s Directory goes out to 30,000 referral sources
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nationwide and the online website receives over 2-million hits each year. SEAK’s Directory
also offers a 100% money back guarantee.
Become certified by the American Board of Independent Medical Examiners and list yourself in
their Directory.
Join the American Academy of Disability Evaluating Physicians and become listed on their web
site directory.
Do a superb job and generate word of mouth referrals and repeat business. You can help
facilitate repeat referrals by personally calling the referrer to thank them for your assignments.
Buy an IME practice. IME practices can be bought and sold. Check for notices from IME
physicians in your area who are looking to retire and sell their IME practices.
11. What equipment, overhead do I need?
The overhead and equipment required is minimal. Office space can be rented on an as needed basis.
Contractors can be used for transcription. Often times IME companies will provide the office space
and transcription services for you. Medical equipment required is generally very basic. The
following instruments are necessary to do proper impairment/IME evaluations:
Stethoscope and blood pressure cuff
Goniometers (small and large)
Finger goniometer
Inclinometers (two)
Grip and pinch strength measuring devices, e.g., a Jamar dynamometer
Tongue blades
Pen light
Tape measure
Reflex hammer
Purdue pegboard
Tuning fork
Cotton balls
Two-point discrimination measuring device, e.g., DiskCriminator
Appropriate text books: (AMA Guides 5th edition/6th edition, Medical Disability Advisor
(MDA), and/or Official Disability Guidelines (ODG), other impairment rating guides as
required in your jurisdiction)
Range of motion text books/booklets: (AMA, American Academy of Orthopedic Surgeons,
etc)
Specific equipment for specialty and subspecialty practices
12. Do you need to become certified to perform IMEs?
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Generally no, but possibly for workers’ compensation IMEs depending on the jurisdiction.
Exactly what “certification” requires in each jurisdiction also varies.
13. Should I become certified by ABIME?
If you are serious about building an IME practice, ABIME certification is a wise investment.
Although there is time and cost involved, it is nothing like what is involved in earning your
primary or underlying board certification. ABIME requires:
Continuing medical education in the performance of independent medical
examinations and disability and impairment evaluation
A selective application process meeting standards of education, experience and
ethical conduct
A signed agreement to abide by professional guidelines of conduct
A competency examination covering such key aspects as clinical competency,
behavioral science, impairment and disability systems, and the AMA Guides to the
Evaluation of Permanent Impairment
Recertification every 5 years
Try doing IMEs for a while and if you enjoy performing them, consider ABIME certification to
increase your skills and the number and type of referrals you receive.
14. What special skills do independent medical examiners have?
In addition to their typical clinical medical knowledge, successful independent medical
examiners are skilled in:
Evaluating impairment under the AMA’s Guides to the Evaluation of Permanent
Impairment or the guidelines in use in the state in question.
Testifying skills. Successful independent medical examiners are able to truthfully and
artfully defend their conclusions during depositions, hearings and trials.
Knowledge of symptom magnification, CRPS-1, CRPS-2, fibromyalgia, chronic pain,
personality disorders and other common controversial conditions and issues.
Knowledge of the workers’ compensation and tort systems.
Ability to conduct a thorough specialty examination in a suitable IME format and
document the results.
Ability to critically analyze conflicting information and form an opinion on key issues,
such as:
o Ability to return to work and in what capacity
o Causation
o Diagnosis
o Disability
o Impairment
o Loss of use
o Prognosis
o Reasonableness of care and medical treatment
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Understanding of medical-legal terminology
15. How often will I have to testify?
If you abhor confrontation and are unwilling to testify, IMEs are not for you. You can expect
that approximately 1 in 20 cases will result in your having to give testimony. Since most
physicians charge at least $500/hour for their time testifying, fees for testifying can be a
lucrative supplement to fees for IMEs.
16. What are the risks of performing IMEs?
You will likely be put under subtle and not so subtle pressure to produce a favorable opinion
and report. Worse, you may sometimes be pressured to change an opinion. If you give in to
these pressures the best case result is that your credibility (and viability as an independent
medical examiner) will sooner or later be destroyed.
It is a rare occurrence, but IME physicians may be successfully sued. Four things to watch
out for are: not having a chaperone when examining the opposite sex, hurting an examinee
during an exam (for example by making the examinee move in such a way that injures
them), not acting appropriately when you discover that the examinee has a previously
unknown serious medical condition, and giving the examinee medical advice, thus creating a
physician-patient relationship.
17. Can I perform IMEs if I am no longer practicing clinical medicine?
Some referral sources prefer or even require physicians who are still practicing clinical
medicine (treating patients). In addition, some jurisdictions require that physicians still be in
active practice. Many physicians satisfy this desire or requirement by practicing a few days a
month. In any event, maintaining an active practice certainly helps an examiner’s credibility.
However, many physicians continue to do IMEs for years after they fully retire or become
disabled from practicing their specialty.
18. Can I perform IMEs in a state where I am not licensed to practice medicine?
Although IMEs are not strictly the practice of medicine (there is no doctor-patient relationship
between the physician and the examinee), most states require medical examiners to be licensed
within that state. Hence you should research this before agreeing to perform out of state IMEs.
19. What are the biggest advantages of performing IMEs?
No call.
No nights or weekends. IMEs are typically conducted during regular business hours.
Relatively little legal risk. Compared to practicing clinical medicine, the legal risk involved
in performing IMEs is minimal.
Significant earning potential.
Paid for no-shows.
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Very low overhead required. See #11, above.
Minimal equipment needed in general.
The intellectual challenge of doing something a little different for a change.
Low start up costs.
Fairly easy to get trained and up-to-speed.
Some referral sources require you to carry medical malpractice insurance but malpractice
carriers often provide lower, e.g., administrative, rates if you are not treating patients, and
may offer part time discounts as well.
Errors and omissions insurance rates are reasonable.
An IME practice of good reputation has sale value if you should decide to retire, or stop
performing IMEs.
20. What are the disadvantages and problems associated with performing IMEs?
It can be stressful. The examinees you deal with may be angry, uncooperative,
dysfunctional, etc. and will often view you as an adversary.
It can be adversarial. You will be deposed in a number of your cases and you can expect
opposing counsel to accuse you of being less than honest.
You will feel pressure to produce favorable opinions/reports.
Some referral sources will not pay you commensurate with the first class job you are
doing.
Because of the adversarial nature of IMEs, examiners not uncommonly have complaints
filed against them by disgruntled examinees. Most of these complaints are baseless and
are summarily disposed of, but this is something you should expect.
You are no longer helping patients get better. You are instead supporting the legal
system, which may be less satisfying.
21. What is the “typical” IME practice like?
It varies.
Some practices are high volume, low cost. A physician may do 10-15 IMEs in a day.
Some practices are low volume, high cost. The focus here would be on high end cases that pay
$5,000 or more.
Many physicians start doing IMEs in their 50s and 60s to plan ahead for the future and make
their schedules more manageable. Gradually they keep cutting down on the clinical work, but
maintain a respectable income with predictable hours doing IMEs.
Many physicians start performing IMEs mid-career to supplement their income, diversify their
practice, and position themselves for the future.
Some physicians get into IMEs as a near full time practice early on as it can be a lucrative
practice with predictable hours.
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Many physically disabled physicians do IMEs when they can no longer perform surgery.
Some IME practices take cases from IME brokers, others do not.
22. Is an IME practice a right fit for me?
Only you can decide this. Truly successful IME physicians are usually those who are not thin
skinned, are well credentialed, do not unduly fear confrontation, and who understand they are
working as part of the legal system.
23. What other valuable skills am I likely to acquire from doing IMEs.
1. You will have an opportunity to testify fairly frequently and become comfortable and
proficient doing so. This skill can help you do more medical expert witness work.
2. You will be positioned to perform disability file reviews for hundreds of dollars per hour.
3. Much of the time involved in IMEs is spent reviewing the examinee’s medical records and
commenting on these in your report. You will hone your skills in doing peer reviews for
Medical Review Organizations. The typical IME physician can earn $85-$120/hour doing
this type of low stress, non-confrontational work
24. Can I perform IMEs where the issue is outside of my specialty?
This is not a good idea.
25. What should I do if I decide to start doing IMEs?
Your first step should be to get some training on how to do IMEs and obtain any necessary
equipment. You should also consider reading one or more texts on IMEs. Once you have a
comfort level regarding what is expected, what to do, and how to do it, sign up with some
IME brokers and referral agencies and see if you like the work. If you do, you can take
further steps to increase your skills, find a niche and obtain cases directly, without use of the
broker or referral company.
Visit www.SupplementalIncomeForPhysicians.com for information on IME Training.
SEAK’s National IME Directory: www.imedirectory.com
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Writing Your File and Disability Reviews
All of the work you will be doing reading records, analyzing records, and researching will ultimately
assist you as the foundation for your written file reviews.
As a physician file reviewer your clients will judge you and make decisions about rehiring you
based on the quality of your written reviews.
Here are some suggestions on how to do a well-written review.
State things clearly and directly
Do not speculate or guess
Avoid boilerplate language
Avoid the use of absolute words (e.g., “always” & “never”)
The review should not be vague, equivocal or uncertain
Avoid emphatic language, exclamation points, boldface, underlining, italics and capital
letters to emphasize points or conclusions
Use active voice
Use precise language
Use confident language that avoids hedge words (e.g., “it seems,” “could,” “apparently,”
and “I believe”)
Define technical terms, jargon and abbreviations
Make sure the report is internally consistent and consistent with any previous reviews of
the file
Avoid evidence of bias
Citation to authority:
Bolster the credibility of the review
Citations should be detailed (title, author, edition, publisher & year published)
Conclusion
The disability and file review practice is a billion dollar industry that is growing rapidly. Clients will
judge you on the quality of your written review so it is crucially important that you hit the ground
running with excellent reviews. Clients will likely only give you once chance to succeed before they
move on to another physician file reviewer.
SEAK runs an annual training program on How to Start, Build, and Run a Successful Disability
and File Review Consulting Practice. For additional information please visit:
www.SupplementalIncomeForPhysicians.com
And if you are interested in performing file reviews, consider joining SEAK’s National Directory
of Medical File Review Consultants; www.FileReviewConsultants.com
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a. A Curriculum Vitae(CV) - This should be drafted very carefully. Keep in mind
that opposing parties will try to use against you the language you utilized in your
CV to present your qualifications, experience, education, etc.
b. A Retention Contract - A well drafted retention contract will prevent
innumerable potential problems and make sure that you get paid. See for
example SEAK’s Expert Witness Retention Contract which is in use by
over 1,500 experts.
The Single Most Important Key to being a Successful Expert Witness: Expert witnessing is a
reputation driven field. Word-of-mouth and repeat business results in the majority of expert
witness referrals. Successful expert witnesses are those who generate positive word-of-mouth. In
order to generate positive word-of-mouth, an expert must excel and be responsive and easy to
deal with. This includes:
a. Exceeding the Expectations of Retaining Counsel.
b. Being Responsive.
c. Being Available.
d. Being Dependable.
e. Having no Credibility Issues.
f. Forming Defensible Opinions.
g. Writing Superior Reports.
h. Excelling at Deposition and Trial.
Getting the Word Out: There are a number of proven ways for expert witnesses to get cases (in
addition to word of mouth). These include:
a. Positioning themselves in a lucrative, growing, and underserved niche.
b. Developing a professional and search engine optimized website for their
expert witness practice.
c. Networking.
d. Listing themselves in expert witness directories such as the SEAK Expert
Witness Directory (www.seakexperts.com).
e. Identifying and reaching out to the select group of attorneys most likely to
retain you.
f. Leveraging professional social media such as Linkedin.
g. Speaking.
h. Publishing.
i. Using third party brokers or referral services such as Roundtable Group,
TASA, or ForensisGroup.
j. Demonstrating leadership in a field.
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The Biggest Mistakes Made in Starting an Expert Witness Practice:
a. Thinking you are not qualified because you didn’t go to Harvard, don’t have a
PhD, and your CV is only one page long. This is a common fallacy that is
simply not true. Expert witnesses are judged by their experience,
performance, testifying skills and street smarts as well as their academic
background.
b. Thinking that you are too young or too old. You don’t need to wait until your
50s or 60s to get started. As long as you feel comfortable with your
knowledge and experience in a field you should be good to go. At the other
end of the spectrum, many successful experts keep doing this work into their
80s and even beyond.
c. Promoting a wide range of areas of expertise. Attorneys don’t want a jack of
all trades master of none. Casting too wide a net is often counterproductive.
Consider focusing on narrower niches.
d. Charging too little. A low ball fee may scare away clients as the client may
assume there is something wrong with you if you charge too low of a fee. e.
Not devoting enough time to your CV. An expert’s CV needs to be perfect.
Spend whatever time necessary and get whatever help you need to make it
so.
f. Not devoting enough time to your web presence. The first thing an attorney
looking to hire you will do is to Google you. Google yourself and take a hard
look at what’s out there. Try to fix anything that would reflect badly on you.
g. Thinking that there is something wrong or unseemly about advertising. This
will cost you a lot of money as advertising can be a very cost-effective way of
getting business. It’s not the fact of advertising that gets experts in trouble,
it’s when experts place ill-considered language in their ads.
Conclusion: Getting into expert witnessing is often described by our clients as a life changing
event. It is very lucrative. You can generate a substantial amount of ongoing income. Most of
the work can be done from home. It is intellectually stimulating and you will learn a lot.
If you are not thin skinned and don’t mind working under deadline and maybe travelling a little,
you might want to strongly consider giving expert witnessing a try.
About SEAK, Inc.:
SEAK is the Expert Witness Training Company. Through our products, services,
seminars, expert witness directory, conferences, and one-on-one consulting, we
assist expert witnesses to start, build, run, and expand their practices.
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Starting the query by saying you are writing because you are looking for an agent. This point
is obvious and need not be repeated, and
Failing to research the agent’s website and following the directions there for query
submission.
SOLUTION
Most agents and agencies have specific guidelines for submissions. Due to the large number of
queries, agents appreciate authors who strictly adhere to their guidelines. Make sure your query
is letter perfect and contains no typographical or other sloppy mistakes.
MISTAKE: Query Too Long
The industry standard for a query letter is one page. Agents appreciate authors who get to the
point, are concise, and can write a one-page query letter. The agent wants to be able to quickly
and efficiently read the queries. The agent wants to see the writing style and ability of the author
reflected in the query. Your ability to hook the agent with style, content, story, plot, and
character in one page will encourage the agent to seek sample chapters from you.
SOLUTION
This is simple: make sure your query letter is one page in length.
MISTAKE: Comparing Your Work to a Classic
Agents are voracious readers and have read and loved many of the classics. When the author gets
carried away describing his unpublished manuscript, it can be a serious mistake and result in the
query being discarded. Examples of authors getting carried away with descriptions/comparisons
include:
Comparing their manuscript to “The Catcher in the Rye” or other classics,
Stating that all the people who have read their novel (families and friends) think it is great,
Stating the novel is unlike any other book ever written,
Stating the book will appeal to everyone,
Praising your work with adjectives like amazing, thrilling, or breath-taking, and
Stating your book is a guaranteed best-seller/NY Times best-seller.
SOLUTION
Do not oversell your book. It does not have to be a classic or even a NY Times best-seller. All it
needs to be is a book the agent believes in and thinks she can sell.
MISTAKE: Making the Query Too Personal
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New authors too often try to use personal information in their query letter to win agents over.
Most agents do not react well to extraneous personal information. Examples of authors getting
too personal include:
Putting your age in,
Telling the agent your life story, and
Explaining how hard the book was to write.
SOLUTION
Do not send photos, candy, gifts, or too much personal information. What the agents are looking
for is a great query and book.
MISTAKE: Failure to Make Yourself Easy to Contact
New authors, in their haste to get out their queries and get their book published, often make it too
difficult for the agent to contact them.
SOLUTION
This is another simple one. Each query should include the author’s full contact information,
including: phone and cell number, email address, and street address.
MISTAKE: Discussing Unpublished Works
New authors often describe, sometimes in detail, all of their unpublished works. This does not
instill confidence in the agent and can result in not making the cut.
SOLUTION
Do not waste valuable space in your query discussing unpublished works, how many years you
have been trying to get published, or apologizing for not already being published. Concentrate
your query on the book you are selling the agent.
MISTAKE: Annoying Links
One of the tell-tale signs of a mass query is the author including links to a website, etc. If you
must include a link, make it easy for the agent to navigate. Remember, the agents are not
computer experts.
SOLUTION
Make sure any attachments/links are well labeled, easy to navigate and add, and not detract from
the power of your query.
MISTAKE: Pitching More Than One Book
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Many new authors cannot resist the temptation to pitch more than one book in their query. Their
thinking is likely that maybe one will catch the eye of the agent. Agents almost universally resent
a query with multiple books, series, etc. They are looking for one book they can sell.
SOLUTION
Authors are best served by limiting the query to one book. If the query is strong enough, the
agent may inquire about additional books.
MISTAKE: Leaving Out Key Information
New authors often try to put every character, plot line, and twist and turn of their novel in the
query. These authors are left with little or no space for key aspects of a successful query, such as:
Having a rock solid two line hook,
Information about platform,
Including key information to help the agent understand how the project is different and better
than what’s on the market,
Clarity about genre or even if it is fiction or non-fiction,
Including sense of characters or themes, and
Describing succinctly what they are pitching.
CONCLUSION
Many new authors do not spend sufficient time and effort in perfecting their query. This is the
most serious mistake a new author can make. To succeed, authors should research literary agents
and send out a select group of queries. The authors should follow the submission guidelines to
the letter. Authors who avoid the common mistakes noted above are best positioned to have a
literary agent take them on as a client.
NOTE: The mistakes and advice listed above are a compilation of the suggested advice of
numerous literary agents who were consulted and asked for their advice for new
authors submitting query letters.