Q4B evaluation and recommendation of pharmacopoeial texts for use in the ICH regions: annex 5(R1) : disintegration test general chapter
- 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, September 2017
- Chemistry, Pharmaceutical -- standards Drug Approval Pharmacopoeias as Topic -- standards Capsules Congresses as Topic International Cooperation Tablets Humans Europe Japan 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 (4 pages)).
- Revision 1
- NLM Unique ID:
- 101713299 (See catalog record)