To keep pace with rapidly changing health care demands, clinical research resources need to be organized and on hand to address the numerous health care questions that continually emerge. Improving the overall capacity of the clinical research enterprise will depend on ensuring that there is an adequate infrastructure in place to support the investigators who conduct research, the patients with real diseases who volunteer to participate in experimental research, and the institutions that organize and carry out the trials.
The workshop, summarized in this volume, laid the foundation for a broader initiative of the Forum addressing different aspects of clinical research. Future Forum plans include further examining regulatory, administrative, and structural barriers to the effective conduct of clinical research; developing a vision for a stable, continuously funded clinical research infrastructure in the United States; and considering strategies and collaborative activities to facilitate more robust public engagement in the clinical research enterprise.
The Role of Purchasers and Payers in the Clinical Research Enterprise: Workshop Summary.
Toon meer Toon minder. English Co-redacteur Robert B. Giffin Uitgever National Academies Press. Reviews Schrijf een review. Bindwijze: Paperback. Successfully reported this slideshow. We use your LinkedIn profile and activity data to personalize ads and to show you more relevant ads. You can change your ad preferences anytime. Upcoming SlideShare. Like this document? Why not share! A view on canada healthcare sector Embed Size px.
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Post- marketing research gives insight into all kinds of questions and concerns raised by the FDA. Not only does it allow companies to monitor for real time effectiveness, long term safety and real-time tolerability, but it may also give rise to evidence of possible new indications and new markets for which the drug product had not been initially approved. Initiatives; , 1 2. Before drugs are marketed, drugs are considered drug candidates.
As you know, these processes can take many, many years, filled with many trials and errors.
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If a drug can candidate has successfully sustained this and makes it way to market, and becomes a drug product, the are many important and unanswered questions that there are, in essence, very time-sensitive. These questions include mainly safety and efficacy concerns sensitive.
How safe and effective is it when used by a patient with more than one illness ness? How does the drug product compare in safety, efficacy and safety, tolerability with other products in its class? Pricing for a pre-ordered book is estimated and subject to change. All backorders will be released at the final established price. If the price decreases, we will simply charge the lower price. Applicable discounts will be extended.
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The eBook is optimized for e-reader devices and apps, which means that it offers a much better digital reading experience than a PDF, including resizable text and interactive features when available. If an eBook is available, you'll see the option to purchase it on the book page. View more FAQ's about Ebooks. Proceedings: Proceedings published by the National Academies of Sciences, Engineering, and Medicine chronicle the presentations and discussions at a workshop, symposium, or other event convened by the National Academies.
The statements and opinions contained in proceedings are those of the participants and are not endorsed by other participants, the planning committee, or the National Academies. In a workshop organized by the Clinical Research roundtable, representatives from purchaser organizations employers , payer organizations health plans and insurance companies , and other stakeholder organizations voluntary health associations, clinical researchers, research organizations, and the technology community came together to explore:.
This book documents these discussions and summarizes what employers and insurers need from and are willing to contribute to clinical research from both a business and a national health care perspective. The National Academies Press and the Transportation Research Board have partnered with Copyright Clearance Center to offer a variety of options for reusing our content.
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