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1. Medical devices

Author(s):

White, Robert S., (Compliance Attorney and member of the Oklahoma Bar), author

Publication:

[Toronto, Ontario] : Thomson Reuters, 19-December-2022

Subject(s):

Device Approval
Product Surveillance, Postmarketing
Equipment Safety
Medical Device Recalls -- legislation & jurisprudence
United States
United States. Food and Drug Administration

2. Initiation of voluntary recalls under 21 CFR Part 7, subpart C: guidance for industry and FDA staff

Publication:

Rockville, MD : Office of Regulatory Affairs, March 2022

Subject(s):

Drug Recalls -- legislation & jurisprudence
Medical Device Recalls -- legislation & jurisprudence
Product Recalls and Withdrawals -- legislation & jurisprudence
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration