Guidance for industry quality systems approach to pharmaceutical CGMP regulations.
| Other Authors: | Center for Drug Evaluation and Research (U.S.), Center for Biologics Evaluation and Research (U.S.), Center for Veterinary Medicine (U.S.), United States. Food and Drug Administration. Office of Regulatory Affairs. |
|---|---|
| Format: | Electronic |
| Language: | English |
| Published: |
Rockville, MD :
U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research,
[2006]
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| Physical Description: |
1 online resource (28 pages) |
| Subjects: | |
| Online Access: |
https://purl.fdlp.gov/GPO/LPS116599 |
https://purl.fdlp.gov/GPO/LPS116599
CMU Gov Pub Electronic
Electronic Resource Click Here| Location | Call Number: | Status |
|---|---|---|
| CMU Gov Pub Electronic | HE 20.4702:Q 1/2 | Available |