# Pharmacogenomic Data Submissions; Examples of Voluntary Submissions or Submissions Required Under 21 CFR 312, 314, or 601 - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/pharmacogenomic-data-submissions-examples-of-voluntary-submissions-or-submissions-required-under-21-cfr-312-314-or-601/097d6c1f-5f70-4be5-acc2-a2029bde4dab

> FDA guidance document: Pharmacogenomic Data Submissions; Examples of Voluntary Submissions or Submissions Required Under 21 CFR 312, 314, or 601. Issue date: March 01, 2005. Get complete insights and analysis.

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## Details

- Title: Pharmacogenomic Data Submissions; Examples of Voluntary Submissions or Submissions Required Under 21 CFR 312, 314, or 601
- Communication Type: Guidance Document
- Product Type: drugs
- Office Name: Center for Drug Evaluation and Research
- Office URL: /offices/center-for-drug-evaluation-and-research/cd980d74-1cbf-4226-ba9a-9045324c236c
- Issue Date: 2005-03-01
- Last Changed: 2019-06-15

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