# Waiver of IRB Requirements for Drug and Biological Product Studies:  Guidance For Sponsors, Clinical Investigators, and IRBs - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/information-sheet/waiver-of-irb-requirements-for-drug-and-biological-product-studies-guidance-for-sponsors-clinical-investigators-and-irbs/409bb967-d13b-4e0e-a277-2a2382de216e

> FDA guidance document: Waiver of IRB Requirements for Drug and Biological Product Studies:  Guidance For Sponsors, Clinical Investigators, and IRBs. Issue date: October 03, 2017. Get complete insights and analysis.

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## Details

- Title: Waiver of IRB Requirements for Drug and Biological Product Studies:  Guidance For Sponsors, Clinical Investigators, and IRBs
- Communication Type: Information Sheet
- Product Type: biologics
- Office Name: Office of the Commissioner
- Office URL: /offices/office-of-the-commissioner/79483979-9582-427f-ac3d-46c715811424
- Issue Date: 2017-10-03
- Last Changed: 2019-04-18

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