Structured Summary
Abstract
Authorization allowing the Food and Drug Administration (FDA) to strengthen public health protections against chemical, biological, radiological, and nuclear threats including infectious diseases, by facilitating the availability and use of medical countermeasures needed during public health emergencies. Under section 564 of the Federal Food, Drug, and Cosmetic Act, FDA may authorize unapproved medical products or unapproved uses of approved medical products to be used in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or agents when certain criteria are met, including there are no adequate, approved, and available alternatives.(From fda.gov/regulatory-information/search-fda-guidance-documents/emergency-use-authorization-medical-products-and-related-authorities)
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Classification
Broader headings
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Synonyms
5 entry terms
- EUA
- Authorization, Emergency Use
- Authorizations, Emergency Use
- Emergency Use Authorizations
- Use Authorization, Emergency
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Aspects Covered
3 allowable subheadings
Indexed with the subheadings economics, history, legislation & jurisprudence.
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History Note
2025
MeSH Hierarchy
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AMA Style
References
- National Library of Medicine. Emergency Use Authorization. Medical Subject Headings (MeSH). 2026. Unique ID D000098485. http://id.nlm.nih.gov/mesh/2026/D000098485
- Emergency Use Authorization. In: Wikipedia. https://en.wikipedia.org/wiki/Emergency_Use_Authorization
- Emergency Use Authorization. In: Wikidata. https://www.wikidata.org/wiki/Q5370662