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Guideline for submitting documentation for the manufacture of and controls for drug products.
- Format:
- Book
- Government document
- Language:
- English
- Subjects (All):
- Drugs--Dosage forms--Quality control--Documentation--United States.
- Drugs.
- Legislation, Drug.
- New drug applications.
- Investigational New Drug Application.
- Pharmaceutical Preparations--manufacture.
- Pharmaceutical Preparations--laws & regulations.
- Technology, Pharmaceutical--legislation & jurisprudence.
- United States.
- Medical Subjects:
- Legislation, Drug.
- New drug applications.
- Investigational New Drug Application.
- Pharmaceutical Preparations--manufacture.
- Pharmaceutical Preparations--laws & regulations.
- Technology, Pharmaceutical--legislation & jurisprudence.
- Physical Description:
- 1 online resource (1 electronic resource (17 pages))
- Other Title:
- Title from cover page: Guidance for industry
- Place of Publication:
- Rockville, Md. : Center for Drugs and Biologics, Food amd [sic] Drug Administration, U.S. Dept. of Health and Human Services, [1987]
- Other Format:
- Print version: Guideline for submitting documentation for the manufacture of and controls for drug products
- OCLC:
- 586027282
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