Collections: Health Policy and Services Research / Subjects: Product Labeling - Digital Collections - National Library of Medicine Search Results

Start Over Collections Health Policy and Services Research ✖ Subjects Product Labeling ✖

1. FDA oversight of tobacco manufacturing establishments

Publication:: [Washington, D.C.] : U.S. Department of Health and Human Services, Office of Inspector General, August 2017
Subject(s):: Government Regulation
Tobacco Industry
Tobacco Products
Advertising as Topic
Product Labeling
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

2. Dangers associated with unlabeled basins, bowls, and cups

Publication:: [Harrisburg, Pa.] : Pennsylvania Patient Safety Authority, March 2005
Subject(s):: Drug Labeling
Medical Errors -- prevention & control
Medication Errors -- prevention & control
Operating Rooms -- methods
Product Labeling
Surgical Equipment
Drug Packaging
Patient Safety
Product Packaging
Humans
Pennsylvania
United States

3. Enforcement policy--OTC sunscreen drug products marketed without an approved application

Publication:: Silver Spring, MD : Center for Drug Evaluation and Research, May 2018
Subject(s):: Health Policy
Marketing
Sunscreening Agents
Consumer Product Safety
Product Labeling
Sun Protection Factor
Humans
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.

4. Medical devices: cancer risk led FDA to warn against certain uses of power morcellators and recommend new labeling : report to Congressional requesters

Publication:: Washington, D.C. : U.S. Government Accountability Office, February 2017
Subject(s):: Device Approval
Equipment Safety
Morcellation -- adverse effects
Morcellation -- instrumentation
Product Labeling
Leiomyoma -- surgery
Uterine Neoplasms -- surgery
Humans
United States
United States. Food and Drug Administration

5. Collaborative patient safety effort: addressing phlebotomy specimen mislabeling

Publication:: [Harrisburg, Pa.] : Pennsylvania Patient Safety Authority, c2009
Subject(s):: Blood Specimen Collection -- methods
Cooperative Behavior
Medical Errors -- prevention & control
Product Labeling
Specimen Handling -- methods
Data Collection
Phlebotomy -- methods
Program Development
Safety
Humans
United States

6. Clear liquids may place patients at risk

Publication:: [Harrisburg, Pa.] : Pennsylvania Patient Safety Authority, [2005]
Subject(s):: Drug Labeling
Medical Errors -- prevention & control
Medication Errors -- prevention & control
Product Labeling
Drug Storage
Patient Safety
Risk Management
Solutions
Humans
Pennsylvania
United States

7. Mix-up between skin prep solution and adhesive remover

Publication:: [Harrisburg, Pa.] : Pennsylvania Patient Safety Authority, [2006]
Subject(s):: Dermatologic Agents
Medical Errors -- prevention & control
Adhesiveness
Electrodes
Patient Safety
Product Labeling
Product Packaging
Solutions -- adverse effects
Humans
Pennsylvania
United States

8. Unique device identification: Policy regarding compliance dates for class I and unclassified devices, direct marking, and Global Unique Device Identification Database requirements for certain devices : guidance for industry and Food and Drug Administration staff

Publication:: Silver Spring, MD : Center for Devices and Radiological Health, July 25, 2022
Subject(s):: Databases as Topic
Equipment and Supplies
Government Regulation
Product Labeling
United States
United States. Food and Drug Administration

9. Instructions for use: patient labeling for human prescription drug and biological products : content and format

Publication:: Silver Spring, MD : Center for Drug Evaluation and Research, July 2022
Subject(s):: Biological Products
Government Regulation
Prescription Drugs
Product Labeling
United States
United States. Food and Drug Administration

10. Unique device identification: policy regarding compliance dates for class I and unclassified devices and certain devices requiring direct marking : immediately in effect guidance for industry and Food and Drug Administration staff

Publication:: Silver Spring, MD : Center for Devices and Radiological Health, July 1, 2020
Subject(s):: Equipment and Supplies -- standards
Medical Device Legislation
Product Labeling
United States
United States. Department of Health and Human Services.
United States. Food and Drug Administration.