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- 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):
- Sanzenbacher, Geoffrey T., author
Wettstein, Gal, author
- Publication:
- Chestnut Hill, MA : Center for Retirement Research at Boston College, May 2019
- Subject(s):
- Drug Costs
Drugs, Generic -- economics
Medicare Part D -- economics
Patents as Topic
Aged
Drug Industry -- economics
Economics, Pharmaceutical
Humans
United States
United States. Food and Drug Administration.
Medical Expenditure Panel Survey (U.S.)
- Author(s):
- White, Robert S., author
- Publication:
- [Toronto, Ontario] : Thomson Reuters, 23-December-2019
- Subject(s):
- Drug Approval
Drug Therapy
Government Regulation
Orphan Drug Production
Rare Diseases -- drug therapy
Humans
United States
United States. Food and Drug Administration.
- Publication:
- Silver Spring, MD : Center for Drug Evaluation and Research, February 1, 2019
- Subject(s):
- Anti-Infective Agents
Device Approval
Drug Approval
Drug Development
Microbial Sensitivity Tests
Drug Industry
Biotechnology
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.
- Publication:
- Silver Spring, MD : Center for Biologics Evaluation and Research, September 20, 2019
- Subject(s):
- Drug Approval
Therapeutic Equivalency
Safety
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.
- Publication:
- Silver Spring, MD : Center for Biologics Evaluation and Research, February 5, 2019
- Subject(s):
- Device Approval
Equipment Safety
Humans
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, June 14, 2019
- Subject(s):
- Device Approval
Equipment and Supplies -- classification
Gastroenterology -- instrumentation
Gynecology
Obstetrics -- instrumentation
Otolaryngology -- instrumentation
Physical and Rehabilitation Medicine -- instrumentation
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.
