Q7 good manufacturing practice guidance for active pharmaceutical ingredients: questions and answers
- Series Title(s):
- Guidance for industry
United States. Department of Health and Human Services, issuing body.
United States. Food and Drug Administration, issuing body.
Center for Biologics Evaluation and Research (U.S.), issuing body.
Center for Drug Evaluation and Research (U.S.), issuing body.
- Silver Spring, MD : Center for Drug Evaluation and Research, April 2018
- Chemistry, Pharmaceutical -- standards Pharmaceutical Preparations -- standards Quality Control Drug Contamination Drug Labeling -- standards International Cooperation Humans United States United States. Department of Health and Human Services. United States. Food and Drug Administration.
- Guideline Technical Report
- The National Library of Medicine believes this item to be in the public domain. (More information)
- 1 online resource (1 PDF file (i, 21 pages)).
- NLM Unique ID:
- 101734165 (See catalog record)