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1A1. A.1.1.1A1A Briefing Document NDA 20920 Cardiovascular and Renal Drugs Advisory Committee Briefing Document () for Injection 25 May 2001 Scion Inc. 820 West Maude Avenue Sunnyvale, California
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Briefing document nda 20-920 is a document required by the National Drug Administration (NDA) for the submission of certain drug-related information.
Any company or party involved in the development, testing, or submission of drugs to the NDA is required to file briefing document nda 20-920.
Filling out briefing document nda 20-920 involves providing the requested information and complying with the specified format and guidelines provided by the NDA.
The purpose of briefing document nda 20-920 is to provide the NDA with relevant information about the drug and its development process, aiding in the evaluation and assessment of its safety and efficacy.
The specific information to be reported on briefing document nda 20-920 may vary depending on the drug, but typically includes details about the drug's formulation, manufacturing process, preclinical and clinical data, and any known risks or side effects.
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