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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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What is briefing document nda 20-920?

Briefing document nda 20-920 is a document required by the National Drug Administration (NDA) for the submission of certain drug-related information.

Who is required to file briefing document nda 20-920?

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.

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Filling out briefing document nda 20-920 involves providing the requested information and complying with the specified format and guidelines provided by the NDA.

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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.

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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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