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Real-world evidence generation and evaluation of therapeutics : proceedings of a workshop /

The volume and complexity of information about individual patients is greatly increasing with use of electronic records and personal devices. Potential effects on medical product development in the context of this wealth of real-world data could be numerous and varied, ranging from the ability to de...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Autor principal: Downey, Autumn S. (rapporteur.)
Autores Corporativos: National Academies of Sciences, Engineering, and Medicine (U.S.). Forum on Drug Discovery, Development, and Translation (sponsoring body.), Real-World Evidence Generation and Evaluation of Therapeutics (Workshop)
Otros Autores: Gee, Amanda Wagner (rapporteur.), Claiborne, Anne B. (rapporteur.)
Formato: Electrónico Congresos, conferencias eBook
Idioma:Inglés
Publicado: Washington, DC : The National Academies Press, [2017]
Colección:Online access: NCBI NCBI Bookshelf.
Temas:
Acceso en línea:Texto completo

MARC

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100 1 |a Downey, Autumn S.,  |e rapporteur. 
245 1 0 |a Real-world evidence generation and evaluation of therapeutics :  |b proceedings of a workshop /  |c Autumn Downey, Amanda Wagner Gee, and Anne B. Claiborne, rapporteurs ; Forum on Drug Discovery, Development, and Translation, Board on Health Sciences Policy, Health and Medicine Division, the National Academies of Sciences, Engineering, Medicine. 
264 1 |a Washington, DC :  |b The National Academies Press,  |c [2017] 
300 |a 1 online resource (1 PDF file (xvi, 85 pages)) :  |b illustrations 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
504 |a Includes bibliographical references. 
520 3 |a The volume and complexity of information about individual patients is greatly increasing with use of electronic records and personal devices. Potential effects on medical product development in the context of this wealth of real-world data could be numerous and varied, ranging from the ability to determine both large-scale and patient-specific effects of treatments to the ability to assess how therapeutics affect patients' lives through measurement of lifestyle changes. In October 2016, the National Academies of Sciences, Engineering, and Medicine held a workshop to facilitate dialogue among stakeholders about the opportunities and challenges for incorporating real-world evidence into all stages in the process for the generation and evaluation of therapeutics. Participants explored unmet stakeholder needs and opportunities to generate new kinds of evidence that meet those needs. This publication summarizes the presentations and discussions from the workshop. 
536 |a This activity was supported by AbbVie Inc.; American Diabetes Association; American Society of Microbiology; Amgen Inc. (Contract No. GHCCOPS-CSARF-85167); Association of American Medical Colleges; AstraZeneca; Baxalta; Burroughs Wellcome Fund (Contract No. 1016598); Critical Path Institute; Eli Lilly & Co.; FasterCures; Friends of Cancer Research; GlaxoSmithKline (Contract No. 016084); Johnson & Johnson; Merck & Co., Inc. (Contract No. CMO-16208-001245); National Institutes of Health (NIH) (Contract No. HHSN263201200074I, Task Order HHSN26300093): National Cancer Institute, National Center for Advancing Translational Sciences, National Institute of Allergy and Infectious Diseases, National Institute of Mental Health, National Institute of Neurological Disorders and Stroke; New England Journal of Medicine; Pfizer Inc.; Sanofi; Takeda Pharmaceuticals (Contract No. 53108); and U.S. Food and Drug Administration (Contract No. 1R13FD005496-01). Any opinions, findings, conclusions, or recommendations expressed in this publication do not necessarily reflect the views of any organization or agency that provided support for the project. 
588 0 |a Online resource; title from PDF title page (viewed August 26, 2017). 
505 0 |a Introduction -- Improving evidence generation for decision making on approval and use of new treatments: some stakeholder priorities -- Opportunities for real-world data -- Generating and incorporating real-world evidence into medical product development and evaluation: building from successful case studies -- Potential strategies for a way forward -- Appendix A: Bibliography -- Appendix B: Workshop agenda -- Appendix C: Participant biographies -- Appendix D: Discussion paper: real-world evidence to guide the approval and use of new treatments. 
590 |a ProQuest Ebook Central  |b Ebook Central Academic Complete 
650 0 |a Evidence-based medicine  |x Data processing  |v Congresses. 
650 1 2 |a Data Mining  |x methods 
650 1 2 |a Evidence-Based Medicine  |x methods 
650 2 2 |a Drug Therapy  |x methods 
650 2 2 |a Electronic Health Records 
650 2 2 |a Therapeutics  |x methods 
650 6 |a Médecine factuelle  |x Informatique  |v Congrès. 
655 2 |a Congress 
655 7 |a proceedings (reports)  |2 aat 
655 7 |a Conference papers and proceedings  |2 fast 
655 7 |a Conference papers and proceedings.  |2 lcgft 
655 7 |a Actes de congrès.  |2 rvmgf 
700 1 |a Gee, Amanda Wagner,  |e rapporteur. 
700 1 |a Claiborne, Anne B.,  |e rapporteur. 
710 2 |a National Academies of Sciences, Engineering, and Medicine (U.S.).  |b Forum on Drug Discovery, Development, and Translation,  |e sponsoring body. 
711 2 |a Real-World Evidence Generation and Evaluation of Therapeutics (Workshop) :  |d (2016 :  |c Washington, D.C.) 
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776 0 8 |i Print version:  |a Downey, Autumn S.  |t Real-world evidence generation and evaluation of therapeutics.  |d Washington, DC : National Academies Press, [2017]  |z 0309455626  |w (OCoLC)973754834 
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