IDSC is an interdisciplinary group of over 55 former pharmaceutical leaders with expertise in drug discovery and development from small molecules and biologics to medical devices. They provide consulting, project management, and integrated collaboration services across therapeutic areas from hit identification to clinical trials. IDSC's clients include biotech, pharma, academia, and venture capital seeking expertise in discovery, preclinical and clinical development to advance their programs.
IDSC is an interdisciplinary group of 40 ex-pharma leaders averaging 25-years of big-pharma, biotech, and academic experience. Our clients come to us for drug discovery and drug development interim leadership, consulting, fully integrated collaborations, due diligence, molecular modeling, and outsourcing management. Because we are a fully integrated drug discovery, preclinical development, and clinical development partner, we help our biotech, VC, academic, and pharma clients get from early discovery to IND filing and through phase I clinical trials in all major therapeutic areas and on to NDA in antibacterials, CNS, and oncology.
Increase quality, decrease stress in a hospital - Pieter E. Buwalda & Gijs An...commonsenseLT
Pieter E. Buwalda, Manager Hospital Operations Programs, Nij Smellinghe Hospital in Drachten (The Netherlands) &
Gijs Andrea, Consultant, implementor, trainer at House of TOC, Education Implementation Management Consultancy (The Netherlands) @ TOCICO International Public Sector Effectiveness Conference 2013 Vilnius
- How to improve the quality of healthcare services using managerial tools.
- How to improve the quality of care AND decrease the workload on nurses and doctors with the same amount of patients treated.
- How to decrease occupation of beds?
- How to decrease length of stay?
More information - http://pse.lt
Vic Chance discusses how Cordis, a Johnson & Johnson company, implemented lean thinking to improve operations. They started by adopting Toyota's production system and focused on eliminating waste. This led to significant results, such as a 150% increase in production volume while reducing floor space, inventory, labor costs, and increasing quality. Lean thinking was then applied to other areas like new facility design, transactional processes, and new product development. Overall, lean provided major wins for Cordis by reducing costs and improving profitability.
SMi Group's Prefilled Syringes East Coast 2018 conferenceDale Butler
This document summarizes a two-day conference on pre-filled syringes taking place in Boston on April 10-11, 2018. The conference will include two pre-conference workshops on human factors for connected drug delivery systems and design considerations for drug delivery outside the clinic. The main conference will focus on challenges and solutions for PFS manufacturing and processes, integrating quality by design principles, and trends toward increasing biologics and their implications for PFS. It will feature speakers from major pharmaceutical companies and include panel discussions on challenges of biologics delivery and PFS development.
This document discusses office-based surgery and its advantages over hospital-based procedures. It notes that over 12 million outpatient surgeries per year are now performed in doctors' offices. Office-based surgery offers higher reimbursements for physicians, more control over scheduling and care, and lower costs and greater convenience for patients. Setting up an office-based surgery center requires considerations around finances, state laws, facility requirements, billing, equipment, staffing, and quality oversight. Choosing experts with experience in multiple clinical and operational areas can help ensure the success of office-based procedural labs.
This document provides information about an upcoming conference on managing partnerships with contract research organizations (CROs). The conference will take place on October 3-4, 2012 in London and will include presentations from pharmaceutical companies and CROs on trends in clinical development outsourcing, developing effective CRO partnerships, and managing regulatory inspections of CRO activities. Pre-conference workshops on October 2 will focus on defining the scope of CRO relationships and ensuring quality in CRO engagements. Key speakers are listed from pharmaceutical companies like Pfizer, Eli Lilly and AstraZeneca and CROs like Quintiles. The document outlines the conference agenda and encourages those in clinical development, outsourcing, and related areas to attend.
IDSC is an interdisciplinary group of 40 ex-pharma leaders averaging 25-years of big-pharma, biotech, and academic experience. Our clients come to us for drug discovery and drug development interim leadership, consulting, fully integrated collaborations, due diligence, molecular modeling, and outsourcing management. Because we are a fully integrated drug discovery, preclinical development, and clinical development partner, we help our biotech, VC, academic, and pharma clients get from early discovery to IND filing and through phase I clinical trials in all major therapeutic areas and on to NDA in antibacterials, CNS, and oncology.
Increase quality, decrease stress in a hospital - Pieter E. Buwalda & Gijs An...commonsenseLT
Pieter E. Buwalda, Manager Hospital Operations Programs, Nij Smellinghe Hospital in Drachten (The Netherlands) &
Gijs Andrea, Consultant, implementor, trainer at House of TOC, Education Implementation Management Consultancy (The Netherlands) @ TOCICO International Public Sector Effectiveness Conference 2013 Vilnius
- How to improve the quality of healthcare services using managerial tools.
- How to improve the quality of care AND decrease the workload on nurses and doctors with the same amount of patients treated.
- How to decrease occupation of beds?
- How to decrease length of stay?
More information - http://pse.lt
Vic Chance discusses how Cordis, a Johnson & Johnson company, implemented lean thinking to improve operations. They started by adopting Toyota's production system and focused on eliminating waste. This led to significant results, such as a 150% increase in production volume while reducing floor space, inventory, labor costs, and increasing quality. Lean thinking was then applied to other areas like new facility design, transactional processes, and new product development. Overall, lean provided major wins for Cordis by reducing costs and improving profitability.
SMi Group's Prefilled Syringes East Coast 2018 conferenceDale Butler
This document summarizes a two-day conference on pre-filled syringes taking place in Boston on April 10-11, 2018. The conference will include two pre-conference workshops on human factors for connected drug delivery systems and design considerations for drug delivery outside the clinic. The main conference will focus on challenges and solutions for PFS manufacturing and processes, integrating quality by design principles, and trends toward increasing biologics and their implications for PFS. It will feature speakers from major pharmaceutical companies and include panel discussions on challenges of biologics delivery and PFS development.
This document discusses office-based surgery and its advantages over hospital-based procedures. It notes that over 12 million outpatient surgeries per year are now performed in doctors' offices. Office-based surgery offers higher reimbursements for physicians, more control over scheduling and care, and lower costs and greater convenience for patients. Setting up an office-based surgery center requires considerations around finances, state laws, facility requirements, billing, equipment, staffing, and quality oversight. Choosing experts with experience in multiple clinical and operational areas can help ensure the success of office-based procedural labs.
This document provides information about an upcoming conference on managing partnerships with contract research organizations (CROs). The conference will take place on October 3-4, 2012 in London and will include presentations from pharmaceutical companies and CROs on trends in clinical development outsourcing, developing effective CRO partnerships, and managing regulatory inspections of CRO activities. Pre-conference workshops on October 2 will focus on defining the scope of CRO relationships and ensuring quality in CRO engagements. Key speakers are listed from pharmaceutical companies like Pfizer, Eli Lilly and AstraZeneca and CROs like Quintiles. The document outlines the conference agenda and encourages those in clinical development, outsourcing, and related areas to attend.
Enhancing the performance of public healthcare systems: achieving more with e...commonsenseLT
Shimeon Pass, expert in Value Enhancement and implementation of advanced management concepts (Israel) @ TOCICO International Public Sector Effectiveness Conference 2013 Vilnius
- Dealing with the complexity of the full scale hospital.
- How can we better synchronize the in-coming stream of patients (from the ER to the internal medicine wards) with the release of patients from wards?
- How do we eliminate the wasted time of physicians and nurses?
- The complete kit concept in ORs, imaging clinics, admission processes and requests for expert opinion.
- Time-based control over the progress of the treatment plan.
- How do we eliminate unnecessary (and risky) waiting times of patients?
More information - http://pse.lt
- The document outlines the initial idea, team, target market size, and interviews conducted for a startup aiming to help oncologists select personalized breast cancer therapies using PET/X technology.
- Over 10 weeks of interviews with 106 participants, the team validated the product-market fit, identified customer segments, and developed initial marketing and financial models.
- Next steps include completing an MVP, partnering with clinical sites, collecting quality data, and submitting a Phase II proposal to further validate the technology and business models.
Sibaya Presentation Drug Delivery Practicebrcocheteux
Sibaya LifeScience provides drug delivery project execution services using a methodology that includes functional analysis, risk analysis, expertise assessment, project management, and hands-on execution. Their expertise includes therapeutics product development, sterilization methods, cGMP compliance, process optimization, and validation. Sibaya aims to identify opportunities, provide insightful advice, and ensure hands-on project execution to exceed client expectations.
Andwin Scientific specializes in Clinical Supplies and Equipment product manufacturing, sourcing, procurement, storage and distribution as a supplier to global life science organizations and a distributor to direct end using companies (including sites). This makes Andwin Scientific the only company that offers true consolidation for clinical studies by facilitating the purchase of products from various suppliers in one transaction.
Cardinal Health is a global healthcare company headquartered in Dublin, Ohio that generates $81 billion in annual revenues. It provides medical products, pharmaceutical distribution services, and clinical technologies to support the healthcare industry. Cardinal Health aims to transform its operations through three priorities: organic growth through customer-driven innovation; leveraging scale and operational excellence to drive superior customer value; and empowering employees. The company pursues operational excellence through a disciplined approach to consistently meet customer expectations with minimum cost and optimum speed. This involves engaging employees at all levels to continuously improve processes through lean techniques. While progress has been made, challenges remain to achieve stability, excellence, and a culture of continuous improvement enterprise-wide.
Karthikeyan Gopal has extensive experience in product design, development, risk management and project management for medical devices. He has worked on projects involving infusion pumps, consumables, combination products and more. His skills include systems engineering, design engineering, validation engineering, risk management, CAD, requirements management, and experience with various medical device standards and regulations. He has held roles at companies such as HCL Technologies, Hospira, American Medical Systems, and Baxter.
Clinical Research Organization Services | Contract Research Company - PepgraPEPGRA Healthcare
Pepgra is a global contract research organization and drug development services company. It provides various phases of clinical research trials services to pharmaceutical and biotechnology companies to help reduce the time and costs associated with drug development.
Contact Us:
Website : https://bit.ly/33Fwsye
Email us: sales.cro@pepgra.com
India: +91 9884350006
United Kingdom: +44- 74248 10299
Orbis Clinical is a specialized consulting firm that provides drug safety, risk management, regulatory, and quality assurance services to pharmaceutical and biotechnology companies. It has experienced consultants with decades of expertise in these areas. Orbis uses a flexible engagement model to quickly respond to clients' needs with individual specialists or broad-based teams.
This article discusses how pathology and diagnostic centers have evolved with new technologies. Modern labs are now digitalized networks that use automation, AI, and other advanced technologies. Tests can now be done from home which is more convenient. Labs are also using new technologies like extended reality in quality control and R&D. Portable point-of-care devices are also improving testing. The future will see more digitally linked devices and home testing that automatically updates medical records. This digital transformation is creating an interconnected healthcare system.
This document provides tips for productive FDA meetings. It advises understanding FDA's perspectives and being flexible in discussions. While FDA aims to innovate, sponsors need to show how their approaches address current needs. Agreement is not always the goal; it is better sometimes to get FDA to tolerate an approach. Meeting minutes may lack clarity, so sponsors should summarize discussion points. Experts and patients at meetings can provide value if well-prepared.
The document discusses lean principles and processes, with a focus on understanding value from the customer's perspective. It emphasizes removing waste, taking a bottom-up approach to identify value and waste, and allowing processes to flow with little command and control. The document also examines how to properly define and measure patient value in healthcare to improve patient experience and outcomes. It argues that current patient satisfaction measures are inadequate and that value should be explored from multiple stakeholder perspectives to guide sustainable service improvements.
The document discusses lessons learned from building a successful electronic health record system in Northern Ireland. It emphasizes that such projects require strong clinical leadership as well as a senior responsible owner. Key building blocks included investing in infrastructure, improving data quality, integrating core clinical applications, and populating the system before going live. Lessons included creating a clinically-led structure, showing users the future benefits, becoming a smart purchaser, and learning exactly what is needed from the system. The goal is for Northern Ireland to have one fully integrated electronic health and care record by 2025.
The Avoca Quality Consortium Summit 2014 Executive SummaryThe Avoca Group
This document provides an executive summary of the 2014 Avoca Quality Consortium Summit. The summit brought together quality, outsourcing, and operational professionals from pharmaceutical, biotech, clinical service providers, and contract research organizations to accelerate the development of best practices for quality management and CRO oversight. The two-day event featured sessions on collaborating with patients, quality by design, insights on quality and effectiveness, and reinventing decision making. It also recognized sponsors Eli Lilly and Company and Pfizer as well as inVentiv Health Clinical for their support. The Avoca Quality Consortium aims to serve as a catalyst for optimizing approaches to proactive quality management and risk mitigation through industry collaboration.
5th Annual Pre-Filled Syringes East CoastTeri Arri
This document provides an agenda for the Pre-Filled Syringes East Coast conference taking place on April 10-12, 2018 in Boston. The agenda includes workshops on human factors for connected drug delivery systems and design considerations for drug delivery outside the clinic on April 10th. The main conference on April 11-12th will feature sessions on regulatory updates, manufacturing challenges and solutions, trends toward biologics, and human factors considerations. Speakers will address topics such as syringe filling of high concentration formulations, safety evaluation of leachables, quality by design principles, and the future of digital monitoring biomarkers.
MedWize Solutions provides services across the drug development process including clinical operations, data management, regulatory affairs, medical writing, and safety to reduce costs and accelerate drug development. They partner with biopharmaceutical companies using innovative technologies and a pay-as-you-go model to improve success rates. Their vision is to provide an industry-leading platform for clinical research and development through data analytics and new technologies.
Image Core lab (ICL) is a premier Imaging service provider exclusively focused on providing high quality specialized imaging service in Bangalore committed to assist Sponsor companies and CRO’s with their imaging requirements as they discover/develop new drug therapies.
IDSC Expertise Capabilities Services Video 2013Mark Creswell
IDSC offers fully integrated drug discovery and development services to biotech, pharma, academic, and VC clients. They have expertise in discovery, preclinical development, clinical development, and project leadership. Their services include medicinal chemistry, pharmacology, ADME/toxicology, API management, clinical development, and regulatory compliance. IDSC has therapeutic area experience in CNS, cardiovascular, oncology, and more. They provide individual experts or fully integrated project teams along with outsourcing management to guide clients' programs from hit identification through clinical development.
Enhancing the performance of public healthcare systems: achieving more with e...commonsenseLT
Shimeon Pass, expert in Value Enhancement and implementation of advanced management concepts (Israel) @ TOCICO International Public Sector Effectiveness Conference 2013 Vilnius
- Dealing with the complexity of the full scale hospital.
- How can we better synchronize the in-coming stream of patients (from the ER to the internal medicine wards) with the release of patients from wards?
- How do we eliminate the wasted time of physicians and nurses?
- The complete kit concept in ORs, imaging clinics, admission processes and requests for expert opinion.
- Time-based control over the progress of the treatment plan.
- How do we eliminate unnecessary (and risky) waiting times of patients?
More information - http://pse.lt
- The document outlines the initial idea, team, target market size, and interviews conducted for a startup aiming to help oncologists select personalized breast cancer therapies using PET/X technology.
- Over 10 weeks of interviews with 106 participants, the team validated the product-market fit, identified customer segments, and developed initial marketing and financial models.
- Next steps include completing an MVP, partnering with clinical sites, collecting quality data, and submitting a Phase II proposal to further validate the technology and business models.
Sibaya Presentation Drug Delivery Practicebrcocheteux
Sibaya LifeScience provides drug delivery project execution services using a methodology that includes functional analysis, risk analysis, expertise assessment, project management, and hands-on execution. Their expertise includes therapeutics product development, sterilization methods, cGMP compliance, process optimization, and validation. Sibaya aims to identify opportunities, provide insightful advice, and ensure hands-on project execution to exceed client expectations.
Andwin Scientific specializes in Clinical Supplies and Equipment product manufacturing, sourcing, procurement, storage and distribution as a supplier to global life science organizations and a distributor to direct end using companies (including sites). This makes Andwin Scientific the only company that offers true consolidation for clinical studies by facilitating the purchase of products from various suppliers in one transaction.
Cardinal Health is a global healthcare company headquartered in Dublin, Ohio that generates $81 billion in annual revenues. It provides medical products, pharmaceutical distribution services, and clinical technologies to support the healthcare industry. Cardinal Health aims to transform its operations through three priorities: organic growth through customer-driven innovation; leveraging scale and operational excellence to drive superior customer value; and empowering employees. The company pursues operational excellence through a disciplined approach to consistently meet customer expectations with minimum cost and optimum speed. This involves engaging employees at all levels to continuously improve processes through lean techniques. While progress has been made, challenges remain to achieve stability, excellence, and a culture of continuous improvement enterprise-wide.
Karthikeyan Gopal has extensive experience in product design, development, risk management and project management for medical devices. He has worked on projects involving infusion pumps, consumables, combination products and more. His skills include systems engineering, design engineering, validation engineering, risk management, CAD, requirements management, and experience with various medical device standards and regulations. He has held roles at companies such as HCL Technologies, Hospira, American Medical Systems, and Baxter.
Clinical Research Organization Services | Contract Research Company - PepgraPEPGRA Healthcare
Pepgra is a global contract research organization and drug development services company. It provides various phases of clinical research trials services to pharmaceutical and biotechnology companies to help reduce the time and costs associated with drug development.
Contact Us:
Website : https://bit.ly/33Fwsye
Email us: sales.cro@pepgra.com
India: +91 9884350006
United Kingdom: +44- 74248 10299
Orbis Clinical is a specialized consulting firm that provides drug safety, risk management, regulatory, and quality assurance services to pharmaceutical and biotechnology companies. It has experienced consultants with decades of expertise in these areas. Orbis uses a flexible engagement model to quickly respond to clients' needs with individual specialists or broad-based teams.
This article discusses how pathology and diagnostic centers have evolved with new technologies. Modern labs are now digitalized networks that use automation, AI, and other advanced technologies. Tests can now be done from home which is more convenient. Labs are also using new technologies like extended reality in quality control and R&D. Portable point-of-care devices are also improving testing. The future will see more digitally linked devices and home testing that automatically updates medical records. This digital transformation is creating an interconnected healthcare system.
This document provides tips for productive FDA meetings. It advises understanding FDA's perspectives and being flexible in discussions. While FDA aims to innovate, sponsors need to show how their approaches address current needs. Agreement is not always the goal; it is better sometimes to get FDA to tolerate an approach. Meeting minutes may lack clarity, so sponsors should summarize discussion points. Experts and patients at meetings can provide value if well-prepared.
The document discusses lean principles and processes, with a focus on understanding value from the customer's perspective. It emphasizes removing waste, taking a bottom-up approach to identify value and waste, and allowing processes to flow with little command and control. The document also examines how to properly define and measure patient value in healthcare to improve patient experience and outcomes. It argues that current patient satisfaction measures are inadequate and that value should be explored from multiple stakeholder perspectives to guide sustainable service improvements.
The document discusses lessons learned from building a successful electronic health record system in Northern Ireland. It emphasizes that such projects require strong clinical leadership as well as a senior responsible owner. Key building blocks included investing in infrastructure, improving data quality, integrating core clinical applications, and populating the system before going live. Lessons included creating a clinically-led structure, showing users the future benefits, becoming a smart purchaser, and learning exactly what is needed from the system. The goal is for Northern Ireland to have one fully integrated electronic health and care record by 2025.
The Avoca Quality Consortium Summit 2014 Executive SummaryThe Avoca Group
This document provides an executive summary of the 2014 Avoca Quality Consortium Summit. The summit brought together quality, outsourcing, and operational professionals from pharmaceutical, biotech, clinical service providers, and contract research organizations to accelerate the development of best practices for quality management and CRO oversight. The two-day event featured sessions on collaborating with patients, quality by design, insights on quality and effectiveness, and reinventing decision making. It also recognized sponsors Eli Lilly and Company and Pfizer as well as inVentiv Health Clinical for their support. The Avoca Quality Consortium aims to serve as a catalyst for optimizing approaches to proactive quality management and risk mitigation through industry collaboration.
5th Annual Pre-Filled Syringes East CoastTeri Arri
This document provides an agenda for the Pre-Filled Syringes East Coast conference taking place on April 10-12, 2018 in Boston. The agenda includes workshops on human factors for connected drug delivery systems and design considerations for drug delivery outside the clinic on April 10th. The main conference on April 11-12th will feature sessions on regulatory updates, manufacturing challenges and solutions, trends toward biologics, and human factors considerations. Speakers will address topics such as syringe filling of high concentration formulations, safety evaluation of leachables, quality by design principles, and the future of digital monitoring biomarkers.
MedWize Solutions provides services across the drug development process including clinical operations, data management, regulatory affairs, medical writing, and safety to reduce costs and accelerate drug development. They partner with biopharmaceutical companies using innovative technologies and a pay-as-you-go model to improve success rates. Their vision is to provide an industry-leading platform for clinical research and development through data analytics and new technologies.
Image Core lab (ICL) is a premier Imaging service provider exclusively focused on providing high quality specialized imaging service in Bangalore committed to assist Sponsor companies and CRO’s with their imaging requirements as they discover/develop new drug therapies.
IDSC Expertise Capabilities Services Video 2013Mark Creswell
IDSC offers fully integrated drug discovery and development services to biotech, pharma, academic, and VC clients. They have expertise in discovery, preclinical development, clinical development, and project leadership. Their services include medicinal chemistry, pharmacology, ADME/toxicology, API management, clinical development, and regulatory compliance. IDSC has therapeutic area experience in CNS, cardiovascular, oncology, and more. They provide individual experts or fully integrated project teams along with outsourcing management to guide clients' programs from hit identification through clinical development.
Hermosillo is the capital city of the state of Sonora, Mexico, located 270km from the US border. It has a population of around 715,000 people and is the 16th largest city in Mexico. The climate is warm desert with average annual temperatures of 25 degrees Celsius. Rain mainly falls during the monsoon season from July to September. The main economic activities are industry, agriculture, livestock, fisheries, and trade.
The document discusses changes in the nursing profession. It notes that there is no longer a single "bedside nurse" as one nurse does not have full care of a patient. Nurses make plans but spend less time at the bedside. The document also mentions that nurses have little freedom in their work and act as go-betweens, with others expecting nurses to fulfill all requests.
This meta-analysis was performed to increase knowledge and understanding on prosthetics and to research what works better for these amputees. This should be used to inform us as clinicians as to what we need to focus on with our amputee patients and what to not overlook throughout the rehabilitation process.
Idsc Expertise Capabilities Services Short 10 Slides 2013 10-09Mark Creswell
IDSC provides drug discovery,preclinical development, clinical development, and outsourcing expertise to assist clients in delivering innovative medicines to the clinic & market faster, while minimizing attrition. We are an interdisciplinary group of 40 ex-pharma leaders averaging 25 years of big pharma experience. Our clients come to us for six main reasons: Drug discovery and development Interim leadership, consulting, fully integrated collaborations, due diligence, molecular modeling, and outsourcing management. Because we are a fully integrated drug discovery, preclinical development, and clinical development partner, we help our biotech, VC, academic, and pharma clients get from early discovery to IND filing and through phase I clinical trials in all major therapeutic areas and on to NDA in antibacterials, CNS, and oncology.
Grade 2+ Ankle Sprain in a Collegiate Football Athletectoney
This document summarizes the rehabilitation process for a collegiate athlete who suffered a grade 2+ ankle sprain. It describes the injury, initial treatment with RICE therapy and bracing, and a 4-stage rehabilitation program focused on restoring range of motion, strength, proprioception, and functional activities. Over 6 weeks the athlete progressed from non-weight bearing to participating in practice activities while continuing rehabilitation exercises and taping for stability. Research supports the benefits of accelerated rehabilitation, taping/bracing for confidence and balance, and restoring ankle range of motion for dynamic balance.
Concussions in high school athletes case study presentationctoney
In the Fall of 2014 I worked as as Athletic Training Student with High School athletes. During this time I evaluated a large amount of athletes with head injuries. This intrigued me to go about research on the topic of concussions.
S.I.C.K. Scapula with Clavicle Fractures Case Study Presentation (2013)ctoney
Each semester as an Athletic Training student we are required to take a clinical course. We are assigned to a clinical site and at the end of each semester we must present on an injury we encountered while working with athletes. Taking further interest into the injury we had to do research. I chose a clavicle fracture because working at a small high school I didn't see many injuries. Once evaluating my patient I realized he had S.I.C.K. Scapula (Scapular Malposition on rib cage, Inferior Medial Scapular Winging, Coracoid Tenderness, Scapular Dyskinesis). After realizing this I continued my research on this condition. I found it to be interesting because I hadn't learned about it in my classes at that point.
Macronutriendes (hidratos de carbono y lípidos)Jimy Cult
Los carbohidratos son moléculas que cumplen funciones energéticas estructurales en los seres vivos. Se clasifican en simples como la glucosa y complejos como el almidón. Proveen la principal fuente de energía para el cuerpo especialmente para el cerebro y sistema nervioso. Los lípidos también son importantes constituyentes de la alimentación que proveen energía y cumplen funciones de reserva, estructurales y de transporte.
This short document contains a link and encourages the reader to click on it to access or obtain something. No other context is provided about what would be received by clicking the link or any other details.
Orbis Clinical is a staffing and consulting company that provides contract professionals focused on drug safety, risk management, clinical operations, medical affairs, regulatory affairs, and quality assurance. They deliver qualified professionals to help clients solve challenges. With offices in Boston, they have served clients nationwide since 2004. Orbis Clinical provides flexible solutions and maintains a bench of qualified resources. Their services include clinical operations support, regulatory submissions and operations assistance, medical affairs support, and quality assurance auditing. Orbis Clinical aims to listen to clients, consult on solutions, and partner with them.
Service Overview
Site management services to CRO and SITE:
A) Pre initiation
Identification of Potential Sites
Faster Feasibility
Site set up, supplies and other infrastructure needs
Regulatory and IEC/ IRB communications
Rapid negotiation of CTA
Setting up Standard Operating Procedures (SOPs)
B) During Study Duration
Provide dedicated trained and experienced CRCs (Clinical research coordinators)
Patient recruitment & retention Support
Maintenance of essential documents
Source documentation as per ALCOA standards (Attributable, Legible, Contemporaneous, Original & Accurate
Regular IP (Investigational Product) accountability and storage
Completion of CRF’s within timelines
Faster query resolution
Reporting of AE, SAEs within timelines
Support Monitoring visits and Quality Assurance audit action items.
Patient visit Follow Up and compliance assistance
Preparation of site for monitoring and audits/ inspections
C) Post Close out
· Archiving of site results and documents
Site Identification
Faster Feasibility
Ready Sites
Genelife Clinical Research is a clinical research organization established in 2010 in Mumbai, India. Their mission is to be the preferred partner for clinical trial sponsors by providing high quality and innovative product development solutions. They offer a full range of clinical research services including operations, data management, statistics, quality assurance, and regulatory affairs. Genelife takes a systematic approach to clinical trials utilizing tools like project management software, EDC systems, and randomization software. They have experience conducting trials across many therapeutic areas for regulators like DCGI, FDA, and TGA. Their differentiating factors include transparent services, advanced techniques, strong regulatory expertise, and a presence in multiple global locations.
Genelife Clinical Research is a clinical research organization established in 2010 in Mumbai, India. Their mission is to be the preferred partner for clinical trial sponsors by providing high quality and innovative product development solutions. They offer a full range of clinical research services including operations, data management, statistics, quality assurance, and regulatory affairs. Genelife takes a systematic approach to clinical trials utilizing tools like project management software, EDC systems, and randomization software. They have experience conducting trials across many therapeutic areas for regulators like DCGI, FDA, and TGA. Their differentiating factors include transparent services, advanced techniques, strong regulatory expertise, and a presence in multiple countries.
We are a Life Science staffing firm focused in the areas of Scientific, Clinical Research & Engineering for the US Biotech, Pharmaceutical, Medical Device and Diagnostic markets.
LED Medical Diagnostics - Investor Presentation April 2014Company Spotlight
LED Medical Diagnostics is expanding into dental imaging with a new division. It has signed partnerships with Ray Co., a Samsung subsidiary, to distribute extraoral imaging systems, and with BC Cancer Agency and Genome BC to develop an oral cancer risk assessment test. The company aims to diversify its product line and grow revenues significantly in 2014 through its existing VELscope business and new digital imaging products. It has a proven management team and is executing its strategic plan through new product launches and sales channel expansion.
Orbis Clinical is a consulting firm focused on providing regulatory affairs, quality assurance, drug safety, and risk management expertise to biopharmaceutical clients. It has over 70 employees and has experienced strong revenue growth. Orbis Clinical delivers flexible, client-driven solutions through engaged consultants and a large virtual bench of additional experts.
CRUCIAL Clinical/Business Consultants matches clinical service providers with sponsors' needs to increase project success. They maintain a portfolio of pre-qualified affiliates in clinical trial services that undergo a comprehensive 20-30 hour qualification process. CRUCIAL promises to act with honesty, understand clients' unique needs, and recommend only providers that are the best fit to ensure clients' success.
Medical Device and Diagnostics Solutions for Every Stage of Your Product's De...Covance
Getting a medical device to the patient takes more than good technology in today's environment. Compelling evidence and convincing value proposition matter. Competing priorities and differing stakeholder definitions of value are driving the need for creative, connected strategies to get the most from each step in the development process. And - as evidence is gathered - it should be used to inform and iterate regulatory, reimbursement and clinical post-market strategies.
TransCelerate Overview - Quality Management System Initiave TransCelerate
TransCelerate BioPharma is a non-profit organization whose mission is to collaborate across the biopharmaceutical industry to identify and implement solutions to improve the delivery of new medicines. The Quality Management System initiative aims to advance quality management across the industry by developing a conceptual framework for clinical quality management systems. The initiative has published several papers outlining its frameworks and tools. Its upcoming milestones include releasing additional tools and publishing additional framework papers on risk management and processes.
Genelife Clinical Research is a technologically advanced CRO that aims to reduce drug development timelines through high quality services. It provides comprehensive clinical trial services from early phase to late phase trials across multiple therapeutic areas globally. Genelife utilizes experienced professionals and innovative tools to efficiently manage projects and ensure quality and regulatory compliance. Its goal is to become the most respected partner in providing product development and meeting unmet clinical research needs.
R&D Partners is a specialty search firm that recruits clinical research and regulatory affairs candidates for pharmaceutical, biotech, diagnostic, and medical device clients. They focus on project management, trial management, monitoring, data management, medical writing, and regulatory affairs positions. R&D Partners prioritizes long-term client relationships based on trust, consistency, and excellence. They have a team of experienced account managers and recruit consultants and permanent hires in areas like clinical research, regulatory affairs, validation, compliance, and quality.
Report : Financial analysis of aanjaneya life careSwapnil Chavan
This document provides a financial analysis report on Aanjaneya Lifecare submitted by Swapnil Chavan and Shreyash Pimparkar. It includes an introduction to the company, certificates of work completion, declarations, preface, acknowledgements, contents, and an overview of the company. The document appears to analyze the financial performance and position of Aanjaneya Lifecare through ratios and annual reports from 2012-2013.
Profound Healthcare Services credentials presentation focusing on projects done with healthcare consulting companies as well as in overall healthcare segment. All projects focus around offerings related to 'Market Intelligence' & 'Process Support'.
Kelly Services provides project services including scalable project development and deployment, customized PMO integration solutions, global talent delivery, industry-specific expertise, and project innovation. They have expertise across industries like engineering, science, IT, oil and energy, mining, and environmental management. Kelly Services uses best-in-class project management methodologies to provide a complete continuum of services including project scoping, feasibility studies, PMO integration, and knowledge transfer to help clients meet objectives and budgets.
This document provides information about Riskpro, an Indian risk management firm. It has offices in major cities and alliances in other cities. Riskpro aims to provide integrated risk consulting services and be a preferred governance, risk and compliance solutions provider. It offers quality advisory services at affordable rates compared to large firms. Riskpro focuses on risk management and has over 200 cumulative years of experience. It provides various risk management and advisory services to healthcare clients, including risk assessments, audits, and training. The document discusses key issues often found in hospitals and Riskpro's internal audit methodology for the healthcare industry.
The document is a term paper analyzing the technical performance of Dr. Reddy's Laboratories, an emerging global pharmaceutical company with businesses in pharmaceutical services, generics, and proprietary products. It provides an overview of Dr. Reddy's capabilities, infrastructure, manufacturing expertise, partnerships, and board of directors. The paper also analyzes the company's financial performance from August 1-15, 2008 based on its daily stock prices.