FDA and industry actions on premarket approval applications (PMAs), effect on FDA review clock and goals
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Contributions
- Center for Biologics Evaluation and Research (U.S.) - Contributor
Publication
2008 - U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health, Rockville, MD], Maryland
Language
English
Word Count
0 words, Guess
Page Count
0 pages
Physical Format
[electronic resource]
Identifiers
- OCLC Control Number351377973
- Open LibraryOL55222060M
Alternate Titles
- Guidance for industry and FDA staff
Subjects
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