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3171. Conduct of clinical trials of medical products during the COVID-19 public health emergency: guidance for industry, investigators, and institutional review boards

Publication:
[Silver Spring, MD] : Center for Drug Evaluation and Research, August 30, 2021
Subject(s):
Clinical Trial Protocols as Topic
Clinical Trials as Topic -- methods
COVID-19
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration

3173. Notifying CDRH of a permanent discontinuance or interruption in manufacturing of a device under Section 506J of the FD&C Act during the COVID-19 public health emergency (revised): guidance for industry and Food and Drug Administration staff

Publication:
[Silver Spring, MD] : Center for Devices and Radiological Health, November 2020
Subject(s):
Equipment and Supplies
Manufacturing Industry
Medical Device Legislation
COVID-19
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration

3177. VA health care: actions needed to ensure provider qualifications and competence : testimony before the Subcommittee on Oversight and Investigations, Committee on Veterans' Affairs, House of Representatives

Publication:
Washington, DC : United States Government Accountability Office, October 2019
Subject(s):
Credentialing
Facility Regulation and Control
Government Regulation
Veterans -- legislation & jurisprudence
United States
United States. Department of Veterans Affairs

3179. Enhancing the diversity of clinical trial populations: eligibility criteria, enrollment practices, and trial designs

Publication:
Silver Spring, MD : Center for Drug Evaluation and Research, November 2020
Subject(s):
Biological Variation, Population
Clinical Trial Protocols as Topic
Clinical Trials as Topic
Population Characteristics
Cultural Diversity
Genetic Variation
United States
United States. Department of Health and Human Services
United States. Food and Drug Administration