This document summarizes a presentation on preparing for meaningful use audits. It provides an overview of recent CMS updates to stage 2 meaningful use requirements, common stumbling blocks providers face, how to conduct a gap analysis, lessons from customer audit experiences, the benefits of mock audits, how intelligent medical objects can help with requirements, and an outlook on future stage 3 goals. Contact information is provided for attendees to ask questions or provide feedback through a post-webcast survey for a chance to win a gift card.
Tips and Tricks on how to go about certifying yourself quickly for the Quality Payment Program in 2018. How does it impact workflow, security and means to accelerate certification.
Clinlogix - Improving Pharmacovigilance Outsourcing with Modern Technologies Veeva Systems
Learn how pharma companies and vendors are collaborating and simplifying processes with modern safety solutions. View the on-demand webinar here: https://bit.ly/30eAlJC
Go deeper with athenahealth specialists to discover all that you need to know and some things you may not know about Meaningful Use Stage 2 and the newest government updates.
Tips and Tricks on how to go about certifying yourself quickly for the Quality Payment Program in 2018. How does it impact workflow, security and means to accelerate certification.
Clinlogix - Improving Pharmacovigilance Outsourcing with Modern Technologies Veeva Systems
Learn how pharma companies and vendors are collaborating and simplifying processes with modern safety solutions. View the on-demand webinar here: https://bit.ly/30eAlJC
Go deeper with athenahealth specialists to discover all that you need to know and some things you may not know about Meaningful Use Stage 2 and the newest government updates.
Tips and Tricks on how to go about certifying yourself quickly for the Quality Payment Program in 2018. How does it impact workflow, security and means to accelerate certification.
Improve care, patient engagement, and efficiency in all areas of your practice with these five fast productivity fixes! You and your staff are sure to benefit from these valuable tips.
MACRA will help us move more quickly towards our goal of value-based care. MIPS combines parts of the Physician Quality Reporting System (PQRS), the Value Modifier (VM or Value-based Payment Modifier), and the Medicare Electronic Health Record (EHR) incentive program into one single program. Have a look at the objectives & measures, quality scoring methodology, clinical practice improvements and other pertinent details.
PICI’s Best Practices for Building Oncology Studies in an EDCVeeva Systems
Watch the video here: https://bit.ly/3vrYslR
The Parker Institute for Cancer Immunotherapy (PICI) runs complex clinical trials that depend on an electronic data capture (EDC) system that is adaptive, flexible and innovating at the same pace as their patient-centric mission.
Learn why their legacy EDC system workarounds and custom functions no longer sustained their business, which motivated them to take a new approach. In this webinar, Toby Odenheim, the Director of Technology and Governance, will share how PICI decided to adopt a new EDC system that streamlines the build process for oncology trials and how they better equip their clinical programmers and data managers. PICI’s lead study builder, Gary Smith, will provide a hands-on perspective and share strategies to handle the key challenges that oncology teams face with EDC systems, including:
* Umbrella trials that evaluate multiple therapies
* Adaptive trial branching and routing
* Having an unknown number of treatment cycles
* Amendments and other unplanned changes
Who Will Benefit:
* Data managers
* Database Programmers
* Clinical Programmers
* Clinical programmers in charge of building studies
* Clinical leaders in charge of selecting EDC systems
* EDC Programmers
Meet Your Presenters:
Toby Odenheim
Director, Technology and Governance, Parker Institute for Cancer Immunotherapy
In his current role as director of technology and governance at PICI, Toby Odenheim, MBA, leads an array of technology and process improvement initiatives aimed at accelerating the development of innovative cancer immunotherapy treatments. Core areas of oversight include management of clinical and pharmacovigilance systems, including CTMS, eTMF, IRT, EDC, ePRO, medical coding, safety, and business intelligence systems.
Prior to joining PICI, Odenheim was the founder and principal at Odin Life Sciences Consulting, where he guided companies in the selection, implementation, and validation of best-of-breed clinical technologies. Toby Odenheim has held management positions at Gilead, Synteract, ClinicalSoft, and Pfizer. He holds an undergraduate degree in biology, an MBA, and professional certifications in finance, Oracle database administration, and relational database design.
Gary Smith
Senior EDC Programmer/Analyst, Parker Institute for Cancer Immunotherapy
Gary has over twenty years of experience in clinical programming and is a subject matter expert on study design, configuration, and testing with off-the-shelf EDC systems including Veeva Vault CDMS, Medidata Rave, and Oracle Clinical. Gary has deep expertise in building oncology studies, specifically platform studies, and is currently responsible for all aspects of EDC design and study builds in immuno-oncology studies with the Parker Institute for Cancer Immunotherapy. Gary has developed global libraries for five different companies, spanning medical device and pharmaceutical industries.
Software Advice BuyerView: Mental Health Software 2014Software Advice
We recently reviewed interactions with mental health software buyers to uncover their most frequent pain points and motivations for purchasing new software.
EHR certification requirements, and the capabilities an EHR should build to be eligible for QPP. Interoperability, data access and security are some of the core of QPP.
Building a Foundation for Proactive and Predictive PharmacovigilanceVeeva Systems
Learn how PV teams can easily keep up with evolving compliance requirements with modern safety applications that provide better data control and drive greater efficiencies.
View on-demand session: https://bit.ly/3vIzQG9
Best practices for implementing and maintaining successful standardsVeeva Systems
Watch the video here: https://bit.ly/3uvar1u
This webinar provides best practices, check-lists and case studies for leveraging standards in clinical trials. From creation and implementation, to governance tools (both internal and with external partners), attendees walk away with actionable insights to leverage with their own organization.
* Understand what to standardize
* Learn several approaches to standards development and when they make sense
* Ensure alignment with key stakeholders
* Maintain and govern standards over time
* Reduce overall configuration time
Who Will Benefit:
* Clinical Data (manager/director/head of) Clinical ops
* Data management
* Biostatistics
* Data science
* Clinical science
* EDC
* Biometrics
* eClinical
* Data standards
* Quantitative sciences
* Informatics
* Data monitoring
* Clinical leads
* Study managers
* Clinical study
* Data manager
* CRA
* CDISC
Meet Your Presenters:
Carla Reis
Director, Client Services, 4G Clinical
Carla Reis, Director of Client Services at 4G Clinical, has over 18 years of experience as an operational leader in developing and implementing RTSM systems in a global pharmaceutical company. Carla was a leader in her organization in establishing vendor management standards and processes. She has helped lead major RTSM process improvement initiatives where she established new and innovated approaches to drug assignment verification and vendor integrations. Carla has presented at industry conferences as a subject matter expert on best practices using RTSM solutions for complex strategies in supply chain management. Carla holds a BS in Neurobiology and Physiology from the University of Connecticut and a certification as Lean Six Sigma Yellow Belt. Carla also holds a Masters in Science in Health Administration with a concentration in Health Informatics from Saint Joseph's University.
Paul MacDonald
Senior Director, Strategy Vault CDMS, Veeva Systems
Paul is Senior Director Vault CDMS, responsible for strategy and direction in data management. With 25+ years experience working in life science at pharma, CRO and technology organisations, Paul brings a strong operational focus in relation to eClinical technology for data management and clinical operations that stretches from EDC, through CTMS to risk based monitoring.
Tufts Research: Strategies from Data Management Leaders to Speed Clinical TrialsVeeva Systems
Watch the video here: https://bit.ly/3wChmGQ
Learn how top pharmas and CROs plan to speed database build and data collection, as well as their top challenges and future priorities. In this webinar you'll gain insights into:
* Taking an agile approach to database build
* Reducing UAT timelines with a risk-based approach
* Driving innovation at your organization
This in-depth research from Tufts follows their industry-wide eClinical Landscape Study, examining the major cause of database build delays and their impact on trial cycle times.
Meet Your Presenters:
Ken Getz
Director of Sponsored Programs, Tufts CSDD
Richard Young
Vice President, Vault EDC, Veeva Systems
The Benefits of a Seamless IRT and EDC Integration in Clinical Trial ExecutionVeeva Systems
Watch the video here: https://bit.ly/3upehbN
Veeva and Suvoda have combined their offerings into a powerful streamlined integration, which accommodates advanced study designs while driving down build and casebook complexity.
Hear Catherine Munera, head of biometrics at Cara Therapeutics, share the benefits of moving from a single provider to taking a harmonized, best-of-breed approach with IRT and EDC.
Speed Clinical Trials from Start to Close: The Path to a Modern CTMSVeeva Systems
Learn how a modern CTMS leads to better oversight, study analytics, and risk identification. This presentation also covers common barriers to the migration process and how to overcome them. Watch a demonstration of Veeva Vault CTMS: http://bit.ly/VaultCTMSDemo
Accelerate and Integrate Digital Health InnovationJohn Reites
4 strategies to influence and execute digital health approaches. Presented on 23 Mar 2016 by John Reites at the Data 4 Decisions Conference in Raleigh, NC.
Collaborate Effectively to Transform Clinical TrialsVeeva Systems
View slides from Veeva's plenary session at ExL's 8th Trial Master File Summit to:
• Learn opportunities to transform trial execution through greater TMF collaboration
• Explore innovative ways to enhance collaboration by automating the exchange of TMF data between sponsors, CROs, and sites
• Learn how to gain and leverage continuous visibility of clinical data exchange to improve oversight, compliance, and decision-making
Improving Clinical Trial Performance: Part 1 - Findings from the Veeva 2018 U...Veeva Systems
Henry Galio shares new findings from the Veeva Unified Clinical Operations Survey showing how clinical leaders are taking action to improve CTMS processes. Access Part II > http://bit.ly/unifyctms_slides
The Industry’s Move Toward Digitally Connected Clinical TrialsVeeva Systems
The rapid adoption of decentralized trials is causing significant challenges – sites are burdened by too many technologies and the use of multiple patient-facing applications adds complexity for patients.
In these slides, we discuss the implications of decentralized trials, share findings from the Veeva Digital Clinical Trials Survey, and explore how clinical leaders are accelerating digital transformation to make studies more site and patient-centric.
Access the Veeva Digital Clinical Trials Survey Report (https://bit.ly/35eAeDn) for additional insights from more than 280 clinical leaders worldwide on the industry’s progress toward digital trial strategies, lessons learned, and what lies ahead.
Reimagine patient safety 2030 governance through a unified safety platformVeeva Systems
Technology disruptions and healthcare transformation are shifting the roles of QPPV's and senior safety leaders to a more predictive, preventative and participatory safety ecosystem.
During the DIA QPPV Forum, Sharmila Sabaratnam, Senior Director Vault Safety Strategy, shared how you can improve collaboration, benefit-risk data flow and quality and generate insights to maximise patient outcome and minimise avoidable harm through medical governance oversight.
For more information visit:
www.veeva.com/eu/products/vault-safety
How to Interpret and Plan for the 2014 CMS CEHRT Rule Iatric Systems
* Flexibility Plan 2014 and what we know
* Mickey Waters, IT Director at Conway Medical Center – Why he chose to take advantage of the rule
* Lyndel Mead, RN, MSN, Clinical Informatics Coordinator at Peterson Regional Medical Center – Why he chose not to take advantage of the rule
* Making the best decision for your organization
* How to get personalized, expert MU advice
MACRA/MIPS Tips: Don't Leave Money on the TableKareo
2022 is the sixth year of the CMS Incentive Program, MACRA /MIPS, and as a practice or billing company, you have seen payment adjustments that have affected your business in more than one way. The biggest impact is payment adjustments, where we see up to a negative 9% of claims paid. So what can you do about it, and how can we minimize those adjustments?
Marina Verdara, CMS Incentive Program SME and Sr. Training Specialist at Kareo will explore what you need to know about MACRA/MIPS and how you can improve your bottom line. She will walk you through:
-The overview of MACRA
-MIPS eligibility, training, and tracking progress for providers
-Billing companies & the claims submission process
-Supporting documentation & attestation
Tips and Tricks on how to go about certifying yourself quickly for the Quality Payment Program in 2018. How does it impact workflow, security and means to accelerate certification.
Improve care, patient engagement, and efficiency in all areas of your practice with these five fast productivity fixes! You and your staff are sure to benefit from these valuable tips.
MACRA will help us move more quickly towards our goal of value-based care. MIPS combines parts of the Physician Quality Reporting System (PQRS), the Value Modifier (VM or Value-based Payment Modifier), and the Medicare Electronic Health Record (EHR) incentive program into one single program. Have a look at the objectives & measures, quality scoring methodology, clinical practice improvements and other pertinent details.
PICI’s Best Practices for Building Oncology Studies in an EDCVeeva Systems
Watch the video here: https://bit.ly/3vrYslR
The Parker Institute for Cancer Immunotherapy (PICI) runs complex clinical trials that depend on an electronic data capture (EDC) system that is adaptive, flexible and innovating at the same pace as their patient-centric mission.
Learn why their legacy EDC system workarounds and custom functions no longer sustained their business, which motivated them to take a new approach. In this webinar, Toby Odenheim, the Director of Technology and Governance, will share how PICI decided to adopt a new EDC system that streamlines the build process for oncology trials and how they better equip their clinical programmers and data managers. PICI’s lead study builder, Gary Smith, will provide a hands-on perspective and share strategies to handle the key challenges that oncology teams face with EDC systems, including:
* Umbrella trials that evaluate multiple therapies
* Adaptive trial branching and routing
* Having an unknown number of treatment cycles
* Amendments and other unplanned changes
Who Will Benefit:
* Data managers
* Database Programmers
* Clinical Programmers
* Clinical programmers in charge of building studies
* Clinical leaders in charge of selecting EDC systems
* EDC Programmers
Meet Your Presenters:
Toby Odenheim
Director, Technology and Governance, Parker Institute for Cancer Immunotherapy
In his current role as director of technology and governance at PICI, Toby Odenheim, MBA, leads an array of technology and process improvement initiatives aimed at accelerating the development of innovative cancer immunotherapy treatments. Core areas of oversight include management of clinical and pharmacovigilance systems, including CTMS, eTMF, IRT, EDC, ePRO, medical coding, safety, and business intelligence systems.
Prior to joining PICI, Odenheim was the founder and principal at Odin Life Sciences Consulting, where he guided companies in the selection, implementation, and validation of best-of-breed clinical technologies. Toby Odenheim has held management positions at Gilead, Synteract, ClinicalSoft, and Pfizer. He holds an undergraduate degree in biology, an MBA, and professional certifications in finance, Oracle database administration, and relational database design.
Gary Smith
Senior EDC Programmer/Analyst, Parker Institute for Cancer Immunotherapy
Gary has over twenty years of experience in clinical programming and is a subject matter expert on study design, configuration, and testing with off-the-shelf EDC systems including Veeva Vault CDMS, Medidata Rave, and Oracle Clinical. Gary has deep expertise in building oncology studies, specifically platform studies, and is currently responsible for all aspects of EDC design and study builds in immuno-oncology studies with the Parker Institute for Cancer Immunotherapy. Gary has developed global libraries for five different companies, spanning medical device and pharmaceutical industries.
Software Advice BuyerView: Mental Health Software 2014Software Advice
We recently reviewed interactions with mental health software buyers to uncover their most frequent pain points and motivations for purchasing new software.
EHR certification requirements, and the capabilities an EHR should build to be eligible for QPP. Interoperability, data access and security are some of the core of QPP.
Building a Foundation for Proactive and Predictive PharmacovigilanceVeeva Systems
Learn how PV teams can easily keep up with evolving compliance requirements with modern safety applications that provide better data control and drive greater efficiencies.
View on-demand session: https://bit.ly/3vIzQG9
Best practices for implementing and maintaining successful standardsVeeva Systems
Watch the video here: https://bit.ly/3uvar1u
This webinar provides best practices, check-lists and case studies for leveraging standards in clinical trials. From creation and implementation, to governance tools (both internal and with external partners), attendees walk away with actionable insights to leverage with their own organization.
* Understand what to standardize
* Learn several approaches to standards development and when they make sense
* Ensure alignment with key stakeholders
* Maintain and govern standards over time
* Reduce overall configuration time
Who Will Benefit:
* Clinical Data (manager/director/head of) Clinical ops
* Data management
* Biostatistics
* Data science
* Clinical science
* EDC
* Biometrics
* eClinical
* Data standards
* Quantitative sciences
* Informatics
* Data monitoring
* Clinical leads
* Study managers
* Clinical study
* Data manager
* CRA
* CDISC
Meet Your Presenters:
Carla Reis
Director, Client Services, 4G Clinical
Carla Reis, Director of Client Services at 4G Clinical, has over 18 years of experience as an operational leader in developing and implementing RTSM systems in a global pharmaceutical company. Carla was a leader in her organization in establishing vendor management standards and processes. She has helped lead major RTSM process improvement initiatives where she established new and innovated approaches to drug assignment verification and vendor integrations. Carla has presented at industry conferences as a subject matter expert on best practices using RTSM solutions for complex strategies in supply chain management. Carla holds a BS in Neurobiology and Physiology from the University of Connecticut and a certification as Lean Six Sigma Yellow Belt. Carla also holds a Masters in Science in Health Administration with a concentration in Health Informatics from Saint Joseph's University.
Paul MacDonald
Senior Director, Strategy Vault CDMS, Veeva Systems
Paul is Senior Director Vault CDMS, responsible for strategy and direction in data management. With 25+ years experience working in life science at pharma, CRO and technology organisations, Paul brings a strong operational focus in relation to eClinical technology for data management and clinical operations that stretches from EDC, through CTMS to risk based monitoring.
Tufts Research: Strategies from Data Management Leaders to Speed Clinical TrialsVeeva Systems
Watch the video here: https://bit.ly/3wChmGQ
Learn how top pharmas and CROs plan to speed database build and data collection, as well as their top challenges and future priorities. In this webinar you'll gain insights into:
* Taking an agile approach to database build
* Reducing UAT timelines with a risk-based approach
* Driving innovation at your organization
This in-depth research from Tufts follows their industry-wide eClinical Landscape Study, examining the major cause of database build delays and their impact on trial cycle times.
Meet Your Presenters:
Ken Getz
Director of Sponsored Programs, Tufts CSDD
Richard Young
Vice President, Vault EDC, Veeva Systems
The Benefits of a Seamless IRT and EDC Integration in Clinical Trial ExecutionVeeva Systems
Watch the video here: https://bit.ly/3upehbN
Veeva and Suvoda have combined their offerings into a powerful streamlined integration, which accommodates advanced study designs while driving down build and casebook complexity.
Hear Catherine Munera, head of biometrics at Cara Therapeutics, share the benefits of moving from a single provider to taking a harmonized, best-of-breed approach with IRT and EDC.
Speed Clinical Trials from Start to Close: The Path to a Modern CTMSVeeva Systems
Learn how a modern CTMS leads to better oversight, study analytics, and risk identification. This presentation also covers common barriers to the migration process and how to overcome them. Watch a demonstration of Veeva Vault CTMS: http://bit.ly/VaultCTMSDemo
Accelerate and Integrate Digital Health InnovationJohn Reites
4 strategies to influence and execute digital health approaches. Presented on 23 Mar 2016 by John Reites at the Data 4 Decisions Conference in Raleigh, NC.
Collaborate Effectively to Transform Clinical TrialsVeeva Systems
View slides from Veeva's plenary session at ExL's 8th Trial Master File Summit to:
• Learn opportunities to transform trial execution through greater TMF collaboration
• Explore innovative ways to enhance collaboration by automating the exchange of TMF data between sponsors, CROs, and sites
• Learn how to gain and leverage continuous visibility of clinical data exchange to improve oversight, compliance, and decision-making
Improving Clinical Trial Performance: Part 1 - Findings from the Veeva 2018 U...Veeva Systems
Henry Galio shares new findings from the Veeva Unified Clinical Operations Survey showing how clinical leaders are taking action to improve CTMS processes. Access Part II > http://bit.ly/unifyctms_slides
The Industry’s Move Toward Digitally Connected Clinical TrialsVeeva Systems
The rapid adoption of decentralized trials is causing significant challenges – sites are burdened by too many technologies and the use of multiple patient-facing applications adds complexity for patients.
In these slides, we discuss the implications of decentralized trials, share findings from the Veeva Digital Clinical Trials Survey, and explore how clinical leaders are accelerating digital transformation to make studies more site and patient-centric.
Access the Veeva Digital Clinical Trials Survey Report (https://bit.ly/35eAeDn) for additional insights from more than 280 clinical leaders worldwide on the industry’s progress toward digital trial strategies, lessons learned, and what lies ahead.
Reimagine patient safety 2030 governance through a unified safety platformVeeva Systems
Technology disruptions and healthcare transformation are shifting the roles of QPPV's and senior safety leaders to a more predictive, preventative and participatory safety ecosystem.
During the DIA QPPV Forum, Sharmila Sabaratnam, Senior Director Vault Safety Strategy, shared how you can improve collaboration, benefit-risk data flow and quality and generate insights to maximise patient outcome and minimise avoidable harm through medical governance oversight.
For more information visit:
www.veeva.com/eu/products/vault-safety
How to Interpret and Plan for the 2014 CMS CEHRT Rule Iatric Systems
* Flexibility Plan 2014 and what we know
* Mickey Waters, IT Director at Conway Medical Center – Why he chose to take advantage of the rule
* Lyndel Mead, RN, MSN, Clinical Informatics Coordinator at Peterson Regional Medical Center – Why he chose not to take advantage of the rule
* Making the best decision for your organization
* How to get personalized, expert MU advice
MACRA/MIPS Tips: Don't Leave Money on the TableKareo
2022 is the sixth year of the CMS Incentive Program, MACRA /MIPS, and as a practice or billing company, you have seen payment adjustments that have affected your business in more than one way. The biggest impact is payment adjustments, where we see up to a negative 9% of claims paid. So what can you do about it, and how can we minimize those adjustments?
Marina Verdara, CMS Incentive Program SME and Sr. Training Specialist at Kareo will explore what you need to know about MACRA/MIPS and how you can improve your bottom line. She will walk you through:
-The overview of MACRA
-MIPS eligibility, training, and tracking progress for providers
-Billing companies & the claims submission process
-Supporting documentation & attestation
Kareo's Regulatory SME and Sr. Training Specialist, Marina Verdara, will walk you through the ABC’s of regulatory programs so you can easily meet your compliance goals and start earning more money for your practice. She will:
-Provide an overview of MACRA
-Breakdown the four MIPS reporting categories, including requirements for each and how you can meet them
-Walk billers and billing companies through the claims submission process
-Share five easy steps to help you earn up to a 9% positive payment adjustment
To provide answers to many questions hospitals and providers have about Meaningful Use in 2015, we’re offering this educational webcast.
This session covers Stage 2 requirements and looks ahead at what’s coming with Stage 3, including:
• Recent updates from CMS
• Keys to successful tracking, attesting, and preparing for an audit
• How to handle difficult measures
• An overview of what we know about Stage 3
As you probably already suspect, choosing the right telemedicine software for your practice is just one step on the road to building a successful telemedicine program. From there, you’ll need to train staff, get your equipment set-up, figure out your workflows, let patients know, and more.
The good news is, the path to building a successful telemedicine program in your practice is often simple once you know the steps.
At eVisit, our team has a lot of experience guiding providers from selecting a telemedicine solution all the way to “launch day,” and making sure the practice is set-up for success. In this presentation, we’ll guide you through the top tips and strategies that you’ll need to build a successful telemedicine program.
You'll Learn:
Common telemedicine workflow mistakes and questions you’ll need to answer
Telemedicine best practices you should implement
Suggestions on equipment set-up and technical tips to know
Strategies for marketing telemedicine to your patients
This presentation was included in an eVisit webinar. Request a recording here: http://try.evisit.com/implementing-telemedicine-your-medical-practice/
Selecting the right Computer Assisted Audit Tool may appear to be a huge undertaking; however, following a systematic approach eases the burden. The right approach minimizes the risk of selecting a product that might not fit into your organization, which could impair your function as it sits underutilized or on the shelf. While point and click visual style tools are settling into the market, many auditors rely on the legacy step-by-step software tools such as ACL, IDEA, Excel and “add-on” tools.
Many chief auditors pursue opportunities to increase the frequency and intensity of interactions with management and realize nothing gets attention faster than finding previously undetected anomalies in company data. Finding the right issues quickly and timely improves the value of audit and can assist audit in winning more work.
Attending this webinar you will learn:
· Identify analysis and financial constraints
· Scoping and defining audit strategic objectives
· Reviewing selection field based on Technical needs
· Building a short/long term on-boarding roadmap
· Realize the lost opportunity of not including all auditors (no auditor left behind)
Practical Strategies for Taking on New Studies Post COVID-19Veeva Systems
Hear expert guidance for ensuring readiness when opening your doors and making data-driven, evidence-based decisions on which studies to accept post COVID-19.
Plan for Success Strategies to Align Reimbursement and Commercialization - OM...April Bright
Product launch is not the time to start securing reimbursement for your device. Reimbursement remains a complex process for orthopaedic companies that could be lessened if properly aligned throughout commercialization. Mr. Hunter shares the who, what and when of reimbursement to ensure that you’ve received proper coverage prior to launch.
Expanding AI in Healthcare: Introducing the New Healthcare.AI™ by Health Cata...Health Catalyst
Healthcare leaders face an unprecedented amount of critical business issues across revenue, cost, and quality. In response, many business and analytics leaders are trying to integrate AI (augmented intelligence) into their analytics processes to better address these critical issues. Leaders have struggled to integrate AI into current tools, integrate or change workflows, and demonstrate a positive impact of AI. We have learned from our first release of Healthcare.ai years ago that it is not enough to have a technically solid, self-service engine for generating and deploying predictive models at the point of care. A more comprehensive approach is needed to successfully use AI.
The New Healthcare.AI offering from Health Catalyst is a transformational suite of products and expert services that address the wider array of critical business issues. Healthcare.AI dramatically broadens the use and uses cases for effective AI within your organization. Join Jason Jones, Chief Analytics and Data Science Officer, as he shares tools and approaches to serve a growing breadth of stakeholders needing faster turnaround and smaller margins for error.
What You’ll Learn:
- How to expand the use cases where AI is applied.
- How to integrate AI into everyday workflow and decisions.
- How to increase your success rate in AI adoption.
EHR Transitions Webinar: Legacy Support & Staff AugmentationJulie Champagne
Whether it’s a massive enterprise-wide EHR transition or the smaller affair of sunsetting a departmental system, the devil of making such projects work is not only in the details, it’s in the people. By that, we mean figuring out who moves, who stays, and how to execute the transition without having a corrupt end product is paramount. But fear not, there are established best practices for navigating every leg of this journey. In this webinar, you’ll hear from one executive who’s made this type of EHR transition odyssey so your trip can be that much smoother.
In this Webinar attendees discussed and learnt about the changes which impact their audit(s). During this Webinar, we discussed:
1. CMS 2015 Program Audit Protocol changes
2. The importance of a correct universe
3. “Monitoring” is not good enough
4. Beneficiary Investigation Analysis (BIA)
Webinar: Integrating Physician Practices into Your NetworkModern Healthcare
As the federal government and private payers move swiftly toward value-based care, hospitals and health systems are increasingly looking to clinical integration strategies as a way to coordinate care more easily across settings, manage the health of populations and take advantage of emerging payment models. Join us as we explore strategies for integrating physician practices and ambulatory care facilities. Our panel of experts will outline proven practices—and pitfalls to avoid—when it comes to growing your network and bringing new docs into the fold.
Similar to Preparation is the Key to Meaningful Use Success (20)
What Covered Entities Need to Know about OCR HIPAA AuditsIatric Systems
Learn how to be better prepared to comply with today's patient privacy rules and regulations.
Hosted by HealthITSecurity.com, you'll get insight directly from HIPAA officer Iliana L. Peters, J.D., LL.M. As senior advisor for HIPAA Compliance and Enforcement, she is today's leading source for understanding HIPAA requirements.
Ms. Peters presents OCR’s 2017 to 2018 goals and objectives and tells you how you can:
-Uncover the patient privacy risks and vulnerabilities in your healthcare organization
-Determine where you can use technology to assist in and encourage consistent compliance
-Manage risk when vendors have access to your patient data
Macra and Hospitalists: Get Your Questions AnsweredIatric Systems
Hospitals still have so many unanswered questions about their requirements for participation in MACRA.
This webinar gives hospitalists an opportunity to ask their questions.
We also cover the following topics:
• MIPS requirements for In-Hospital Physicians
• MIPS program components
• Impact on payments
• Individual and group reporting
• CMS June 30, 2017 deadline
• How to get help defining your plan
How MEDITECH Hospitals Can Meet The New eCQM Reporting Requirements using QRDAIatric Systems
Learn how our QRDA Assist team can prepare you to start capturing data on eight eCQMs as required by CMS.
The ruling went into effect on January 1 of this year, so don't miss learning how you can:
- Select the eCQMs for electronic reporting
- Conduct a gap assessment to determine the current state of the QRDA-1 format
- Get expert guidance for MEDITECH Best Practice interpretation
- Be successful with your QRDA validation and testing in QualityNet Pre-Submission Validation Application (PSVA)
- Take advantage of the ARRA Report Manager
Mac McMillan on how to prepare your organization for an OCR HIPAA AuditIatric Systems
In this session, Mac McMillan provided several key takeaways that healthcare providers and vendors need to know before they receive an OCR audit letter.
Portals, Mobile Devices, and Patient EngagementIatric Systems
Why aren't patients engaging in their own healthcare? Let's explore why they aren't, and changes that will encourage patients to engage in their healthcare. Frank Fortner, President at Iatric Systems, discusses these topics on an HISTalk Tweet chat.
If you’re joining an HIE, watch this webcast to learn the many ways that you can save development time, and reduce the cost of implementing and managing an HIE.
Understanding HL7 version 2.5.1 and Meaningful Use data considerationsIatric Systems
You know that not doing Meaningful Use correctly can impact your incentives. In this Webcast you'll learn what is needed to support HL7 v2.5.1 and its impact on Meaningful Use data exchange.
Improving the Patient Experience with HIT WebcastIatric Systems
Learn how to improve patient experience, weave patient-facing HIT and engagement protocols into your plans, and create a roadmap to improve patient care.
3 Ways to Overcome Your Interface ChallengesIatric Systems
Even though your interface projects may be pushed aside for other high profile IT priorities, we have 3 ways to help you overcome your interface challenges. You’ll learn 3 ways that you can:
• Make your interface projects a priority with a solid plan
• Overcome top challenges of interface implementation
• Handle lack of interface staff resources
5 Ways to Keep Your Interface Projects Under ControlIatric Systems
In this presentation you’ll find out how you can get your hospital interface projects completed on time and on budget. Learn how we can help you:
• Get interfaces built efficiently
• Deploy higher quality interfaces
• Increase staff productivity
MUSE Successfully Navigating the HIE LandscapeIatric Systems
What is HIE? The verb means the electronic sharing of health-related information among organizations and the act of data sharing or exchange. The noun HIE indicates an organization that provides services to enable sharing of health-related information. It also means Health Information Organization (HIO or HIEO). The presentation comes from former hospital CIO Rick Edwards, currently the director of Integration Strategy at Iatric Systems.
Navigating Challenges: Mental Health, Legislation, and the Prison System in B...Guillermo Rivera
This conference will delve into the intricate intersections between mental health, legal frameworks, and the prison system in Bolivia. It aims to provide a comprehensive overview of the current challenges faced by mental health professionals working within the legislative and correctional landscapes. Topics of discussion will include the prevalence and impact of mental health issues among the incarcerated population, the effectiveness of existing mental health policies and legislation, and potential reforms to enhance the mental health support system within prisons.
India Clinical Trials Market: Industry Size and Growth Trends [2030] Analyzed...Kumar Satyam
According to TechSci Research report, "India Clinical Trials Market- By Region, Competition, Forecast & Opportunities, 2030F," the India Clinical Trials Market was valued at USD 2.05 billion in 2024 and is projected to grow at a compound annual growth rate (CAGR) of 8.64% through 2030. The market is driven by a variety of factors, making India an attractive destination for pharmaceutical companies and researchers. India's vast and diverse patient population, cost-effective operational environment, and a large pool of skilled medical professionals contribute significantly to the market's growth. Additionally, increasing government support in streamlining regulations and the growing prevalence of lifestyle diseases further propel the clinical trials market.
Growing Prevalence of Lifestyle Diseases
The rising incidence of lifestyle diseases such as diabetes, cardiovascular diseases, and cancer is a major trend driving the clinical trials market in India. These conditions necessitate the development and testing of new treatment methods, creating a robust demand for clinical trials. The increasing burden of these diseases highlights the need for innovative therapies and underscores the importance of India as a key player in global clinical research.
Leading the Way in Nephrology: Dr. David Greene's Work with Stem Cells for Ki...Dr. David Greene Arizona
As we watch Dr. Greene's continued efforts and research in Arizona, it's clear that stem cell therapy holds a promising key to unlocking new doors in the treatment of kidney disease. With each study and trial, we step closer to a world where kidney disease is no longer a life sentence but a treatable condition, thanks to pioneers like Dr. David Greene.
CHAPTER 1 SEMESTER V - ROLE OF PEADIATRIC NURSE.pdfSachin Sharma
Pediatric nurses play a vital role in the health and well-being of children. Their responsibilities are wide-ranging, and their objectives can be categorized into several key areas:
1. Direct Patient Care:
Objective: Provide comprehensive and compassionate care to infants, children, and adolescents in various healthcare settings (hospitals, clinics, etc.).
This includes tasks like:
Monitoring vital signs and physical condition.
Administering medications and treatments.
Performing procedures as directed by doctors.
Assisting with daily living activities (bathing, feeding).
Providing emotional support and pain management.
2. Health Promotion and Education:
Objective: Promote healthy behaviors and educate children, families, and communities about preventive healthcare.
This includes tasks like:
Administering vaccinations.
Providing education on nutrition, hygiene, and development.
Offering breastfeeding and childbirth support.
Counseling families on safety and injury prevention.
3. Collaboration and Advocacy:
Objective: Collaborate effectively with doctors, social workers, therapists, and other healthcare professionals to ensure coordinated care for children.
Objective: Advocate for the rights and best interests of their patients, especially when children cannot speak for themselves.
This includes tasks like:
Communicating effectively with healthcare teams.
Identifying and addressing potential risks to child welfare.
Educating families about their child's condition and treatment options.
4. Professional Development and Research:
Objective: Stay up-to-date on the latest advancements in pediatric healthcare through continuing education and research.
Objective: Contribute to improving the quality of care for children by participating in research initiatives.
This includes tasks like:
Attending workshops and conferences on pediatric nursing.
Participating in clinical trials related to child health.
Implementing evidence-based practices into their daily routines.
By fulfilling these objectives, pediatric nurses play a crucial role in ensuring the optimal health and well-being of children throughout all stages of their development.
CHAPTER 1 SEMESTER V PREVENTIVE-PEDIATRICS.pdfSachin Sharma
This content provides an overview of preventive pediatrics. It defines preventive pediatrics as preventing disease and promoting children's physical, mental, and social well-being to achieve positive health. It discusses antenatal, postnatal, and social preventive pediatrics. It also covers various child health programs like immunization, breastfeeding, ICDS, and the roles of organizations like WHO, UNICEF, and nurses in preventive pediatrics.
Global launch of the Healthy Ageing and Prevention Index 2nd wave – alongside...ILC- UK
The Healthy Ageing and Prevention Index is an online tool created by ILC that ranks countries on six metrics including, life span, health span, work span, income, environmental performance, and happiness. The Index helps us understand how well countries have adapted to longevity and inform decision makers on what must be done to maximise the economic benefits that comes with living well for longer.
Alongside the 77th World Health Assembly in Geneva on 28 May 2024, we launched the second version of our Index, allowing us to track progress and give new insights into what needs to be done to keep populations healthier for longer.
The speakers included:
Professor Orazio Schillaci, Minister of Health, Italy
Dr Hans Groth, Chairman of the Board, World Demographic & Ageing Forum
Professor Ilona Kickbusch, Founder and Chair, Global Health Centre, Geneva Graduate Institute and co-chair, World Health Summit Council
Dr Natasha Azzopardi Muscat, Director, Country Health Policies and Systems Division, World Health Organisation EURO
Dr Marta Lomazzi, Executive Manager, World Federation of Public Health Associations
Dr Shyam Bishen, Head, Centre for Health and Healthcare and Member of the Executive Committee, World Economic Forum
Dr Karin Tegmark Wisell, Director General, Public Health Agency of Sweden
Welcome to Secret Tantric, London’s finest VIP Massage agency. Since we first opened our doors, we have provided the ultimate erotic massage experience to innumerable clients, each one searching for the very best sensual massage in London. We come by this reputation honestly with a dynamic team of the city’s most beautiful masseuses.
Telehealth Psychology Building Trust with Clients.pptxThe Harvest Clinic
Telehealth psychology is a digital approach that offers psychological services and mental health care to clients remotely, using technologies like video conferencing, phone calls, text messaging, and mobile apps for communication.
1. Technical Assistance: 978-674-8121 or Amanda.Howell@iatric.com
Audio Options:
Telephone: 1-647-497-9387 | Access Code: 427-057-706
Computer Microphone & Speakers
This teleconference will be muted while we wait for all attendees to join.
Thank you for your patience.
Welcome!
Preparation is the Key
to Meaningful Use
Success
Presented by:
Kay Jackson
(978) 805-3104
Kay.Jackson@iatric.com
Cindy Paul
(978) 674-5927
Cindy.Paul@iatric.com
2. Technical Assistance
•Call 978-674-8121
•Email amanda.howell@iatric.com
How you can participate today
•Collapse and expand your Control Panel
•Select your preferred audio mode
•Submit text questions
Survey
•Please complete the short survey at the end of the
webcast. Your feedback is important to us!
Webcast Guidelines
3. Our Presenters
Kay Jackson
Manager, Software Certification,
Compliance Application Software
Iatric Systems, Inc.
Kay.Jackson@iatric.com
Cindy Paul
Consultant
Professional Services
Iatric Systems, Inc.
Cindy.Paul@iatric.com
Mike Elvin
Consultant
Professional Services
Iatric Systems, Inc.
Mike.Elvin@iatric.com
4. Agenda
Recent updates from CMS and what they mean to you
Stumbling Blocks for Stage 2
Meaningful Use Gap Analysis – do you know where you
stand?
Audits: Customer Examples and How to Prepare
Mock Audits and Beyond
Intelligent Medical Objects (IMO) – what you need to
know for Meaningful Use
A look ahead at MU3
5. Recent Updates from CMS
Stage 2
NPRM- Meaningful Use proposed change for 2014
http://1.usa.gov/1pndpQQ
6. Recent Updates from CMS
Stage 2
• 5/27/14 - CMS published a new proposed rule
that would let providers use 2011 Edition
CEHRT or a combination of 2011 and 2014
CEHRT for the reporting period in 2014
• Beginning 2015 all would be required to
report using 2014 CEHRT
• 60 Day comment period before final rule is
determined – comments due by July 21
• You have the opportunity to comment – 636
comments received (as of 7/17/14)
• Expected to announce the final rule Sept 1
• To Comment, go here: http://1.usa.gov/1pndpQQ
9. What should your team do?
Stage 2 Proposed Rule
1. Review the changes and make comments by 7/21
2. Review the chart and consider a Plan B
3. Move forward with Plan A, but make sure Plan B is ready
4. Use the CEHRT NPRM tool to validate your Plan B
10. CQM 2014
Questions and Answers
• Are we required to submit eCQM data if we reported by the
aggregate method via the CMS attestation tool?
Answer: No, it’s not required
• What is QRDA Cat 3 vs. QRDA Cat 1?
• When are the 2015 rules going to be out?
Answer: 2015 rules are expected to be published in August 2014
• What final advice do you have for 2014 CQMs?
Answer: Be prepared — all coding ready
11. Stumbling Blocks
• Patient Portal- what does CMS really want you to track for
providing access to the portal?
The CMS definition of “access” for this
measure explicitly states that a patient has
access when they possess “all of the
necessary information needed to view,
download, or transmit their
information.” If the patient does not have
“access,” the information cannot be
considered “available” to the patient.
Having a data feed to a portal without
telling patients how to access the portal
doesn’t count.
Response from:
Erica Galvez, MA
Stage 2
14. Stage 2 Core 12
Keys to Success
• Core 12.1 — can be both paper and
electronic
• Core 12.1 and Core 12.2 — can limit by
discharge disposition code
• Is your HIE or HITSP ready?
• Direct Mailbox
• Message Delivery Notification
15. Why there are Meaningful
Use “Gaps”
• Meaningful Use “takes a village”
• Most hospitals have limited resources in
one area or another
• Project management is often difficult and
costly to the hospital
• MU requires C-level buy-in
16. Conducting a Meaningful
Use Gap Analysis
• Offers guidance and suggestions for best
practices in MU objectives and data
capture
• Provides “Gap Analysis Report” to identify
specific areas of improvement to meet
CMS regulations
17. Audits: Customer Experiences
• Audits becoming more frequent and Congress requests more
than 1 in 20 providers
• I am seeing more and more the person who did the attestation
is no longer at the hospital — email audit notification
• Remember the 5 Stage 1 MUST haves — retain for 6 years:
• Letter from all providers of software used in the CHPL
process
• Letter to explain your Method
• Supporting documentation for Cores 1,3,4,5,6,7,8, 11
and 12-report from your EHR system that ties to the
attestation numbers
• Proof of the security risk analysis- see CMS document for
expectations — remediation plan is key
• Supporting documentation for Menu 2,3,5,6 and 7 that
were used to attest as well supporting documentation for
Menu 4,8,9,or 10
Lessons Learned
18. Audits: Customer Experiences
• Are you prepared to respond to a audit? If you fail what
happens?
• Security Risk Analysis:
Resource: CMS Guide to Privacy and Security of Health Information
Lessons Learned
19. Audits: How to Prepare
• Plan “when we are audited, not if”
• Have at least three team members that know where
everything to support the audit is located
• When you attest — have an Attestation Team
• Watch for Notice:
20. Audit Concerns
• Many hospitals believe they are ready…
• Need to be certain all objectives are well
documented
• Often hospitals have holes that are
uncovered during actual audit
• Audit places strain on staff during process
21. Mock Audits
Benefits of a Mock Audit from a third party:
•Team of experts have prior experience
•Ensures proper documentation is provided
•Experts are able to view entire MU reporting
similar to actual audit
•Offer tips on how to best handle audit to
maintain staff efficiencies
22. Going Beyond Mock Audits
Reach beyond MU with patient experience:
•Are patients using their portal or HIE?
•Are they satisfied with physician/provider
communication after their stay?
•Were their discharge instructions adequate?
Did they receive a callback?
•Are they supplied with specific,
comprehensive educational resources?
•Is there room for improvement with
available HIT applications?
23. Intelligent Medical Objects
• Intelligent Medical Objects (IMO):
partnership with EHR vendors to
standardize medical terminology
• IMO integration is essential to populate
accurate:
• Problem Lists
• CQM reporting
• Data fields for CCD, Public health
reporting, Patient Portal and correct
abstract/billing
24. Help for IMO
• Working with IMO can take up to 6
months
• 3rd
Party Vendor can cut this time to 2-3
months
• Familiarity with IMO implementation steps
and procedures
• Additional benefits:
• First-time accuracy reconciling terms
• ROI by reduced internal resources
required for IMO
• External experts have IMO experience
25. Stage 3 EH Delayed
until 10/1/16
Stage 3 Goal is to improve outcomes:
• Hospitals must receive provider-requested, electronically
submitted patient-generated health information through either
structured questionnaires or input from patients
• Hospitals to send electronic notifications of significant healthcare
events to a patient’s care team—such as their primary care
provider, referring provider, or care coordinator — within four
hours of the event. Significant events that would trigger a
notification include:
• Arrival to ED
• Admission to hospital
• Discharge from ED or hospital
• Death
http://bit.ly/1sz1e4Y
27. Meaningful Use
Contact Us | Survey
Survey says:
Please take the survey that appears when you close your
Internet Browser after this webcast. You could win a $100
Amazon.com Gift Card.
Follow us:
For more information:
Please contact your Iatric Systems Account Executive
or send an email to info@iatric.com
Thank you for attending!
Editor's Notes
Leading Meaningful Use preparedness is an overwhelming experience! It takes a village…Hospital IS staff, Clinical Analysts, Nursing Staff, Quality Improvement staff, Medical Records, Admissions, Abstracting & Coding, just to name a few. Many hospitals are limited in staff resources and time to manage this imperative initiative.
Project Management can be simplified with the help of consulting services.
Consultants will interview team members to assess MU readiness
Consultants will offer guidance & suggestions for best practices in accomplishing MU objectives & capturing data
Consultants will provide a Gap Analysis report to identify areas for improvement to meet CMS regulations
Kay – customer stories (customer story: person that did the attestation is no longer there)
Kay – we will send CMS Guide to Privacy and Security of Health Information
Kay (verify where this screenshot is from? CMS website?)
Cindy - Hospitals may believe they’re ready for a Meaningful Use audit…but is there the certainty that all objectives are well documented & confidence that you’ll pass an audit?
Cindy
Cindy
Cindy:
Intelligent Medical Objects – partnership with EHR vendors to standardize medical terminology for Meaningful Use reporting. IMO integration is essential to populate accurate Problem Lists, CQM reporting, and data fields required for the CCD (Continuity of Care Document), Public Health reporting, Patient Portal, and correct abstracting/billing.
When hospital IS staff work with Meditech & IMO Project Managers, implementation & reconciliation of terms can take up to 6 months, depending on staffing resources.
Working with an outside vendor can reduce this time to 2-3 months
Project Management & consulting offers expertise for first time accuracy when reconciling terms
Project Management will provide Return of Investment up front, saving hospital staff from extra meetings & overtime costs which could result from the extra time necessary for IMO implementation
Project Management consultants are familiar with IMO implementation steps & procedures
Cindy:
Intelligent Medical Objects – partnership with EHR vendors to standardize medical terminology for Meaningful Use reporting. IMO integration is essential to populate accurate Problem Lists, CQM reporting, and data fields required for the CCD (Continuity of Care Document), Public Health reporting, Patient Portal, and correct abstracting/billing.
When hospital IS staff work with IMO Project Managers, implementation & reconciliation of terms can take up to 6 months, depending on staffing resources.
Working with an outside vendor can reduce this time to 2-3 months
Project Management & consulting offers expertise for first time accuracy when reconciling terms
Project Management will provide Return of Investment up front, saving hospital staff from extra meetings & overtime costs which could result from the extra time necessary for IMO implementation
Project Management consultants are familiar with IMO implementation steps & procedures