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Start Over Formats Text ✖ Collections Health Policy and Services Research ✖ Subjects United States ✖ Subjects Government Regulation ✖ Copyright Public domain ✖ Recently Added Within 6 Months ✖

1. ACF should improve oversight of head start to better protect children’s safety

Publication:: Washington, D.C. : U.S. Department of Health and Human Services, Office of Inspector General, September 2022
Subject(s):: Child Health
Government Regulation
Early Intervention, Educational
United States
United States. Administration for Children and Families

2. Addressing the direct care workforce shortage: a bipartisan call to action

Publication:: Washington, DC : Bipartisan Policy Center, December 2023
Subject(s):: Emigrants and Immigrants
Government Regulation
Health Policy
Health Workforce
Home Care Services
Home Health Aides
Home Health Nursing
Medicare
United States

3. Adverse events in hospitals. A quarter of Medicare patients experienced harm in October 2018

Publication:: Washington, D.C. : U.S. Department of Health and Human Services, Office of Inspector General, May 2022
Subject(s):: Government Regulation
Hospitals
Medicare
Patient Harm -- prevention & control
Patient Harm -- statistics & numerical data
Patient Safety
United States

4. Adverse events toolkit. Clinical guidance for identifying harm

Publication:: Washington, D.C. : U.S. Department of Health and Human Services, Office of Inspector General, July 2023
Subject(s):: Evaluation Studies as Topic
Government Regulation
Medical Errors
Patient Harm
Risk Management
United States

5. Adverse events toolkit. Medical record review methodology

Publication:: Washington, D.C. : U.S. Department of Health and Human Services, Office of Inspector General, July 2023
Subject(s):: Evaluation Studies as Topic
Government Regulation
Medical Errors
Medical Records
Patient Harm
Risk Management
United States

6. Annual status report information and other submissions for postmarketing requirements and commitments: using forms FDA 3988 and FDA 3989 : guidance for industry

Publication:: Silver Spring, MD : Center for Drug Evaluation and Research, September 2023
Subject(s):: Forms as Topic
Government Regulation
Product Surveillance, Postmarketing
United States
United States.
United States.

7. Antimicrobial susceptibility test (AST) system devices: updating breakpoints in device labeling : guidance for industry and Food and Drug Administration staff

Publication:: Silver Spring, MD : Center for Devices and Radiological Health, September 29, 2023
Subject(s):: Government Regulation
Medical Device Legislation
Microbial Sensitivity Tests -- standards
Product Labeling
United States

8. Antiviral drugs: Economic incentives and strategies for pandemic preparedness : report to congressional committees

Publication:: Washington, DC : United States Government Accountability Office, September 2023
Subject(s):: Antiviral Agents -- economics
Antiviral Agents -- supply & distribution
Government Regulation
Legislation, Medical
Pandemic Preparedness
Technology Assessment, Biomedical
United States

9. Application of human factors engineering principles for combination products: questions and answers : guidance for industry and FDA staff

Publication:: Silver Spring, MD : Center for Devices and Radiological Health, September 2023
Subject(s):: Bioengineering
Device Approval
Drug Development
Drug Industry
Ergonomics
Government Regulation
United States

10. Assessing the credibility of computational modeling and simulation in medical device submissions: guidance for industry and Food and Drug Administration staff

Publication:: [Silver Spring, MD] : Center for Devices and Radiological Health, November 17, 2023
Subject(s):: Computer Simulation
Device Approval
Government Regulation
United States

11. Benefit-risk assessment for new drug and biological products: guidance for industry

Publication:: Silver Spring, MD : Center for Biologics Evaluation and Research, October 2023
Subject(s):: Biological Products
Drug Approval
Drug Industry
Drugs, Investigational
Government Regulation
Pharmaceutical Preparations
Risk Assessment
United States

12. Breakthrough Devices Program: guidance for industry and Food and Drug Administration staff

Publication:: Silver Spring, MD : Center for Devices and Radiological Health, September 15, 2023
Subject(s):: Data Collection
Device Approval
Government Regulation
Medical Device Legislation
United States
United States.
United States.

13. CARES Act: experts identified safeguards to help selected HHS agencies protect against potential political interference : report to congressional requesters

Publication:: Washington, DC : United States Government Accountability Office, September 2023
Subject(s):: Government Regulation
Legislation, Medical
Politics
Professional Misconduct
United States
United States.
United States. Department of Health and Human Services

14. CDC has improved the nursing home reporting process for COVID-19 Data in NHSN, but challenges remain

Publication:: Washington, D.C. : U.S. Department of Health and Human Services, Office of Inspector General, January 2024
Subject(s):: COVID-19
Data Collection
Government Regulation
Mandatory Reporting
Nursing Homes
United States
Centers for Disease Control (U.S.)

15. CDC provided oversight and assistance: however, ELC recipients still faced challenges in implementing COVID-19 screening testing programs

Publication:: [Washington, D.C.] : U.S. Department of Health and Human Services, Office of Inspector General, September 2023
Subject(s):: COVID-19 Testing -- instrumentation
Government Programs
Government Regulation
United States
Centers for Disease Control and Prevention (U.S.)

16. CDC’S Vaccines for Children program recipients did not conduct site visits at some providers as required

Publication:: [Washington, D.C.] : U.S. Department of Health and Human Services, Office of Inspector General, September 2023
Subject(s):: Child Health
Government Programs
Government Regulation
Immunization Programs
Vaccines -- supply & distribution
United States
Centers for Disease Control and Prevention (U.S.)
Vaccines for Children (Program)

17. CDC’s internal control weaknesses led to its initial COVID-19 test kit failure, but CDC ultimately created a working test kit

Publication:: [Washington, D.C.] : U.S. Department of Health and Human Services, Office of Inspector General, October 2023
Subject(s):: COVID-19 Testing -- instrumentation
Equipment Failure Analysis
Government Regulation
United States
Centers for Disease Control and Prevention (U.S.)

18. CMS can do more to leverage Medicare claims data to identify unreported incidents of potential abuse or neglect

Publication:: [Washington, D.C.] : U.S. Department of Health and Human Services, Office of Inspector General, November 2023
Subject(s):: Child Abuse -- legislation & jurisprudence
Elder Abuse -- legislation & jurisprudence
Government Regulation
Medicare -- statistics & numerical data
Vulnerable Populations -- legislation & jurisprudence
United States
Centers for Medicare & Medicaid Services (U.S.)

19. CMS has opportunities to strengthen states’ oversight of Medicaid Managed Care Plans’ reporting of medical loss ratios

Publication:: Washington, D.C. : U.S. Department of Health and Human Services, Office of Inspector General, September 2022
Subject(s):: Government Regulation
Managed Care Programs -- organization & administration
Medicaid
State Health Planning and Development Agencies
United States
Centers for Medicare & Medicaid Services (U.S.)

20. CMS should bolster its oversight of manufacturer-submitted average sales price data to ensure accurate Part B drug payments

Publication:: Washington, D.C. : U.S. Department of Health and Human Services, Office of Inspector General, December 2022
Subject(s):: Cost Control
Drug Costs
Drug Industry
Government Regulation
Medicare Part B
Prescription Fees
United States
Centers for Medicare & Medicaid Services (U.S.)

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