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- Publication:
- Washington, DC : United States Government Accountability Office, December 2017
- Subject(s):
- Device Approval -- standards
Equipment Safety
Federal Government
Forecasting
Government Regulation
Inservice Training
Humans
United States
United States. Food and Drug Administration.
- Publication:
- Washington, DC : United States Government Accountability Office, December 2017
- Subject(s):
- Drug Approval
Drugs, Generic
Therapeutic Equivalency
Chemistry, Pharmaceutical
Doxorubicin
Drug Development
Enoxaparin
Glatiramer Acetate
Gluconates
Propofol
Humans
United States
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:
- Washington, D.C. : AARP Public Policy Institute, c2007
- Subject(s):
- Health Policy -- economics
Cost-Benefit Analysis -- methods
Government Regulation
Federal Government
Decision Making
Delivery of Health Care
Government Agencies
Public Health
Quality-Adjusted Life Years
Safety
Value of Life
Humans
United States
United States. Environmental Protection Agency.
United States. Food and Drug Administration.
- Publication:
- [Harrisburg, Pa.] : Pennsylvania Patient Safety Authority, c2012
- Subject(s):
- Equipment Contamination -- prevention & control
Equipment Reuse
Equipment Safety
Injections -- adverse effects
Pharmaceutical Preparations -- supply & distribution
Humans
Pennsylvania
United States
United States. Food and Drug Administration.
- Author(s):
- Purvis, Leigh, author
- Publication:
- Washington, D.C. : AARP Public Policy Institute, September 2014
- Subject(s):
- Biological Products -- economics
Biological Products -- therapeutic use
Biosimilar Pharmaceuticals -- economics
Biosimilar Pharmaceuticals -- therapeutic use
Drug Costs
Drug Substitution
Legislation, Drug
Drugs, Generic -- economics
Federal Government
State Government
Humans
United States
United States. Food and Drug Administration.
United States.
- Author(s):
- White, Robert S., author
- Publication:
- [Toronto, Ontario] : Thomson Reuters, 21-December-2020
- Subject(s):
- Drug Approval -- organization & administration
Government Regulation
United States
United States. Food and Drug Administration.
- Author(s):
- White, Robert S., author
- Publication:
- [Toronto, Ontario] : Thomson Reuters, 21-December-2020
- Subject(s):
- Device Approval
Equipment Safety
United States
United States. Food and Drug Administration.
- Publication:
- [Silver Spring, MD] : United States Food and Drug Administration, Oncology Center of Excellence, July 2020
- Subject(s):
- Breast Neoplasms
Clinical Trials as Topic
Neoadjuvant Therapy
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.
- Publication:
- [Silver Spring, MD] : Center for Devices and Radiological Health, Office of Product Evaluation and Quality, July 2020
- Subject(s):
- Culture Media
Specimen Handling
Transportation
Virus Diseases
COVID-19
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.