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ElectronicResource GovDoc
Title
Guideline for submitting documentation for the manufacture of and controls for drug products [electronic resource].
Imprint
Rockville, Md. : Center for Drugs and Biologics, Food amd [sic] Drug Administration, U.S. Dept. of Health and Human Services, [1987]
Connect to
Connect to https://permanent.fdlp.gov/lps121022/ucm070630.pdf
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Location
Call No.
OPAC Message
Status
Axe Federal Documents Online
HE 20.4702:D 65
---
Available
Description
1 electronic resource (17 p.)
Note
"Center for Drug Evaluation and Research"--Cover p.
"February 1987."
Subject
Drugs -- Dosage forms -- Quality control -- Documentation -- United States.
Added Author
Center for Drugs and Biologics (U.S.)
Center for Drug Evaluation and Research (U.S.)
Note
Title from cover page: Guidance for industry
Other Form:
Print version: Guideline for submitting documentation for the manufacture of and controls for drug products (OCoLC)16196381
Gpo Item No.
0499-T (online)
Sudoc No.
HE 20.4702:D 65
Available items only
