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.
| Other Authors: | Center for Drug Evaluation and Research (U.S.) |
|---|---|
| Format: | Electronic |
| 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 |