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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 /
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...
| Clasificación: | Libro Electrónico |
|---|---|
| Autor principal: | |
| Autores Corporativos: | , |
| Otros Autores: | , |
| Formato: | Electrónico Congresos, conferencias eBook |
| Idioma: | Inglés |
| Publicado: |
Washington, DC :
National Academies Press,
[2017]
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| Temas: | |
| Acceso en línea: | Texto completo |
MARC
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| 100 | 1 | |a Boname, Morgan L., |e rapporteur. | |
| 245 | 1 | 0 | |a Building a national capability to monitor and assess medical countermeasure use during a public health emergency : |b going beyond the last mile: proceedings of a workshop / |c Morgan Boname, Theresa Wizemann, and Justin Snair, rapporteurs ; Board on Health and Science Policy, Health and Medicine Division, the National Academies of Sciences, Engineering, Medicine. |
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| 520 | 3 | |a 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. | |
| 536 | |a This project was supported by a contract between the National Academy of Sciences and the U.S. Department of Health and Human Services' U.S. Food and Drug Administration (Contract No. 1R13FD005495-01). 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 February 16, 2018). | |
| 505 | 0 | |a Introduction and overview -- Setting the stage : defining terminologies and sharing stakeholder perspectives -- Data needs, data sources, and collection methodologies for stakeholder decision making -- Considerations for conducting rapid clinical research on MCMs during a PHE -- Inspiring collective action : perspectives from federal stakeholders and reflections from individual workshop participants. | |
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| 650 | 0 | |a Patient monitoring |z United States |v Congresses. | |
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