Medical product communications that are consistent with the FDA-required labeling: questions and answers
- Collection:
- Health Policy and Services Research
- Series Title(s):
- Guidance for industry
- Contributor(s):
- United States. Department of Health and Human Services, issuing body. United States. Food and Drug Administration, issuing body. United States. Food and Drug Administration. Office of the Commissioner, issuing body. Center for Biologics Evaluation and Research (U.S.), issuing body. Center for Devices and Radiological Health (U.S.), issuing body. Center for Drug Evaluation and Research (U.S.), issuing body. Center for Veterinary Medicine (U.S.), issuing body.
- Publication:
- Silver Spring, MD : Center for Drug Evaluation and Research, June 2018
- Language(s):
- English
- Format:
- Text
- Subject(s):
- Communication Drug Labeling -- standards Product Labeling -- standards Equipment and Supplies -- standards Pharmaceutical Preparations -- standards Humans United States United States. Department of Health and Human Services. United States. Food and Drug Administration.
- Genre(s):
- Guideline Technical Report
- Copyright:
- The National Library of Medicine believes this item to be in the public domain. (More information)
- Extent:
- 1 online resource (1 PDF file (20 pages)).
- NLM Unique ID:
- 101734292 (See catalog record)
- Permanent Link:
- http://resource.nlm.nih.gov/101734292