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GUIDANCE DOCUMENT

Material Threat Medical Countermeasure Priority Review Vouchers - Draft Guidance for Industry Draft Guidance for Industry January 2018

Draft

Not for implementation. Contains non-binding recommendations.

Docket Number:
FDA-2017-D-6880
Issued by:
Guidance Issuing Office
Office of the Commissioner, Office of the Chief Scientist, Office of Counterterrorism and Emerging Threats

This guidance provides information on implementation of section 3086 of the 21st Century Cures Act (Cures Act) (Public Law 114-255), which added section 565A of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. 360bbb-4a). Section 565A of the FD&C Act requires FDA to award a priority review voucher (PRV) to sponsors of certain medical countermeasure (MCM) applications that meet the criteria specified in that section. Since the enactment of the Cures Act, the Agency has received inquiries about the scope of section 565A of the FD&C Act, its relation to other PRV programs, and how various aspects of section 565A of the FD&C Act should be interpreted. The purpose of this guidance is to provide responses to those questions.


Submit Comments

You can submit online or written comments on any guidance at any time (see 21 CFR 10.115(g)(5))

If unable to submit comments online, please mail written comments to:

Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852

All written comments should be identified with this document's docket number: FDA-2017-D-6880.

 
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