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FDA's drug review process and the package label: strategies for writing successful FDA submissions

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This title provides guidance to pharmaceutical companies for writing FDA-submissions, such as the NDA, BLA, clinical study reports, and investigator's brochures.

The author provides guidance to medical writers for drafting FDA-submissions in a way more likely to persuade FDA reviewers to grant approval of the drug.

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Product Details
Academic Press
0128146486 / 9780128146484
eBook (Adobe Pdf, EPUB)
13/12/2017
English
625 pages
Copy: 10%; print: 10%
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