Building a National Capability to Monitor and Assess Medical Countermeasure Use During a Public Health Emergency
Going Beyond the Last Mile: Proceedings of a Workshop
Board on Health Sciences Policy author National Academies of Sciences, Engineering, and Medicine author Health and Medicine Division author Theresa Wizemann editor Justin Snair editor Morgan, me Bona editor
Format:Paperback
Publisher:National Academies Press
Published:20th Jan '18
Currently unavailable, and unfortunately no date known when it will be back
During public health emergencies (PHEs) involving chemical, biological, radiological, or nuclear threats or emerging infectious diseases, medical countermeasures (MCMs) (e.g., drugs, vaccines, devices) may need to be dispensed or administered to affected populations to help mitigate the human health impact of the threat. The optimal MCMs determined for use during an emergency might be U.S. Food and Drug Administration (FDA) approved but used in unapproved ways (e.g., in a new age group or against a new agent); FDA approved using animal models because human efficacy testing is not ethical or feasible; or not yet FDA approved for any indication.
As part of the United States' scientific and research preparedness enterprise, there is an imperative to go "beyond the last mile" of MCM dispensing and administration to build and maintain a national capability to monitor and assess the use of MCMs (e.g., safety, compliance, clinical benefit) after they have been dispensed during PHEs. To further the discussion on this need, the Board on Health Sciences Policy of the National Academies of Sciences, Engineering, and Medicine hosted a 2-day public workshop, Building a National Capability to Monitor and Assess Medical Countermeasure Use in Response to Public Health Emergencies. The workshop, sponsored by FDA, was held on June 6-7, 2017, in Washington, DC. Workshop participants discussed the roles and efforts of the federal government and of relevant stakeholders with an interest in building and maintaining a national PHE MCM active monitoring and assessment capability. This publication summarizes the presentations and discussions from the workshop.
Table of Contents- Front Matter
- 1 Introduction and Overview
- 2 Setting the Stage: Defining Terminologies and Sharing Stakeholder Perspectives
- 3 Data Needs, Data Sources, and Collection Methodologies for Stakeholder Decision Making
- 4 Considerations for Conducting Rapid Clinical Research on MCMs During a PHE
- 5 Inspiring Collective Action: Perspectives from Federal Stakeholders and Reflections from Individual Workshop Participants
- Appendix A: References
- Appendix B: Workshop Agenda
- Appendix C: Biographical Sketches of Workshop Speakers and Moderators <
ISBN: 9780309466424
Dimensions: unknown
Weight: unknown
120 pages