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1. The "deemed to be a license" provision of the BPCI Act: questions and answers

Publication:: Silver Spring, MD : Center for Drug Evaluation and Research, March 2020
Subject(s):: Biological Products
Drug Approval
Licensure
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

2. "I swear by Apollo physician--": Greek medicine from the gods to Galen

Publication:: [Bethesda, Md. : Medical Arts and Photography Branch, National Institutes of Health, 2002]
Subject(s):: History of Medicine
Exhibits as Topic
History, Ancient
Greece
Galen.

3. ["Tree of Hippocrates" plaque]

Author(s):: Greenberg, Stephen J., photographer
Publication:: Bethesda, MD : U.S. National Library of Medicine, National Institutes of Health, Health & Human Services, [2017]
Subject(s):: Trees
National Library of Medicine (U.S.)

4. The 'New Federalism' and Public Health: Keynote Address to the 18th Annual Conference of the New England Public Health Association, Wychmere Harbor, Cape Cod, Massachusetts [Reminiscence]

Publication:: Produced: 2003
Archival Collection:: The C. Everett Koop Papers (Profiles in Science)

5. The 2018 long-term budget outlook

Publication:: Washington, D.C. : Congressional Budget Office, June 2018
Subject(s):: Budgets -- trends
Federal Government
Forecasting
Medicare -- economics
Medicare -- trends
Social Security -- economics
Social Security -- trends
Humans
United States

6. The 2019 long-term budget outlook

Publication:: [Washington, DC] : Congressional Budget Office, June 2019
Subject(s):: Budgets -- trends
Gross Domestic Product -- trends
Demography
Federal Government
Forecasting
Medicare -- economics
Medicare -- trends
Social Security -- economics
Social Security -- trends
Humans
United States

7. 30-Day notices, 135-day premarket approval (PMA) supplements and 75-day humanitarian device exemption (HDE) supplements for manufacturing method or process changes: guidance for industry and Food and Drug Administration staff

Publication:: Silver Spring, MD : Center for Devices and Radiological Health, December 16, 2019
Subject(s):: Device Approval -- standards
Equipment and Supplies -- standards
Manufactured Materials -- standards
Device Approval -- legislation & jurisprudence
Time Factors
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.
United States.

8. 340B Drug Discount Program: oversight of the Intersection with the Medicaid Drug Rebate Program needs improvement : report to Congressional requesters

Publication:: Washington, DC : United States Government Accountability Office, January 2020
Subject(s):: Drug Costs -- legislation & jurisprudence
Government Regulation
Medicaid -- economics
United States
United States. Department of Health and Human Services

9. 510(k) third party review program: guidance for industry, Food and Drug Administration staff, and third party review organizations

Publication:: Silver Spring, MD : Center for Devices and Radiological Health, March 12, 2020
Subject(s):: Device Approval
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

10. ACF cannot ensure that all child victims of abuse and neglect have court representation

Publication:: Washington, D.C. : U.S. Department of Health and Human Services, Office of Inspector General, March 2021
Subject(s):: Child Abuse -- legislation & jurisprudence
Child Protective Services -- standards
Government Regulation
Legal Services -- organization & administration
United States
United States. Department of Health and Human Services

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