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- Publication:
- Silver Spring, MD : Center for Devices and Radiological Health, August 31, 2017
- Subject(s):
- Equipment and Supplies
Equipment Safety
Evidence-Based Medicine
Product Surveillance, Postmarketing
Data Collection
Data Interpretation, Statistical
Decision Making
Device Approval
Quality Control
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.
- Author(s):
- Lind, Keith D., author
- Publication:
- Washington, DC : AARP Public Policy Institute, August 2017
- Subject(s):
- Government Regulation
Prostheses and Implants -- adverse effects
Prostheses and Implants -- standards
Clinical Trials as Topic
Device Approval
Equipment Failure
Equipment Safety
Product Surveillance, Postmarketing
Registries
Humans
United States
United States. Food and Drug Administration.
- Publication:
- Silver Spring, MD : Office of Counterterrorism and Emerging Threats, May 2020
- Subject(s):
- Dietary Supplements -- adverse effects
Drug-Related Side Effects and Adverse Reactions
Equipment Design -- adverse effects
Equipment Safety
Product Surveillance, Postmarketing
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.
- 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