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A01=and Translation
A01=Board on Health Sciences Policy
A01=Development
A01=Forum on Drug Discovery
A01=Forum on Medical and Public Health Preparedness for Catastrophic Events
A01=Institute of Medicine
Age Group_Uncategorized
Age Group_Uncategorized
Author_and Translation
Author_Board on Health Sciences Policy
Author_Development
Author_Forum on Drug Discovery
Author_Forum on Medical and Public Health Preparedness for Catastrophic Events
Author_Institute of Medicine
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B01=Anne B. Claiborne
B01=Bruce M. Altevogt
B01=Theresa Wizemann
Category1=Non-Fiction
Category=MBP
Category=MMK
COP=United States
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Language_English
PA=Available
Price_€20 to €50
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Advancing Regulatory Science for Medical Countermeasure Development: Workshop Summary

Whether or not the United States has safe and effective medical countermeasuressuch as vaccines, drugs, and diagnostic toolsavailable for use during a disaster can mean the difference between life and death for many Americans. The Food and Drug Administration (FDA) and the scientific community at large could benefit from improved scientific tools and analytic techniques to undertake the complex scientific evaluation and decision making needed to make essential medical countermeasures available. At the request of FDA, the Institute of Medicine (IOM) held a workshop to examine methods to improve the development, evaluation, approval, and regulation of medical countermeasures.

During public health emergencies such as influenza or chemical, biological, radiological/nuclear (CBRN) attacks, safe and effective vaccines, treatments, and other medical countermeasures are essential to protecting national security and the well being of the public. Advancing Regulatory Science for Medical Countermeasure Development examines current medical countermeasures, and investigates the future of research and development in this area. Convened on March 29-30, 2011, this workshop identified regulatory science tools and methods that are available or under development, as well as major gaps in currently available regulatory science tools.

Advancing Regulatory Science for Medical Countermeasure Development is a valuable resource for federal agencies including the Food and Drug Administration (FDA), the Department of Health and Human Services (HHS), the Department of Defense (DoD), as well as health professionals, and public and private health organizations.

Table of Contents
  • Front Matter
  • 1 Introduction
  • 2 MCM Enterprise and Stakeholder Perspectives
  • 3 Cutting-Edge Efforts to Advance MCM Regulatory Science
  • 4 MCM Regulatory Science Needs for At-Risk Populations
  • 5 Crosscutting Themes and Future Directions
  • 6 Closing Remarks
  • References
  • Appendix A: Workshop Agenda
  • Appendix B: Participant Biographies
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A01=and TranslationA01=Board on Health Sciences PolicyA01=DevelopmentA01=Forum on Drug DiscoveryA01=Forum on Medical and Public Health Preparedness for Catastrophic EventsA01=Institute of MedicineAge Group_UncategorizedAuthor_and TranslationAuthor_Board on Health Sciences PolicyAuthor_DevelopmentAuthor_Forum on Drug DiscoveryAuthor_Forum on Medical and Public Health Preparedness for Catastrophic EventsAuthor_Institute of Medicineautomatic-updateB01=Anne B. ClaiborneB01=Bruce M. AltevogtB01=Theresa WizemannCategory1=Non-FictionCategory=MBPCategory=MMKCOP=United StatesDelivery_Delivery within 10-20 working daysLanguage_EnglishPA=AvailablePrice_€20 to €50PS=Activesoftlaunch
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Product Details
  • Dimensions: 152 x 229mm
  • Publication Date: 27 Aug 2011
  • Publisher: National Academies Press
  • Publication City/Country: United States
  • Language: English
  • ISBN13: 9780309214902

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