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Guidance for industry immediate release solid oral dosage forms : scale-up and postapproval changes, chemistry, manufacturing and controls, in vitro dissolution testing, and in vivo bioequivalence documentation.

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Bibliographic Details
Corporate Author: Center for Drug Evaluation and Research (U.S.)
Format: Government Document Electronic eBook
Language:English
Published: [Rockville, Md.] : Center for Drug Evaluation and Research, [1995]
Physical Description:
1 electronic resource (26, 1 page)
Subjects:
Online Access:https://purl.fdlp.gov/GPO/LPS121078
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Holdings details from CMU Gov Pub Electronic C502
Copy 1 CMU Gov Pub Electronic HE 20.4702:D 74/5 Online

Internet

https://purl.fdlp.gov/GPO/LPS121078
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