# CVM GFI #117 (VICH GL24) Management of Adverse Event Reports (AER's) - FDA Guidance Document

Source: https://www.globalkeysolutions.net/guidances/guidance-document/cvm-gfi-117-vich-gl24-management-of-adverse-event-reports-aers/85cb1a62-a46b-4390-a406-c37214267d87

> FDA guidance document: CVM GFI #117 (VICH GL24) Management of Adverse Event Reports (AER's). Issue date: May 01, 2006. Get complete insights and analysis.

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## Details

- Title: CVM GFI #117 (VICH GL24) Management of Adverse Event Reports (AER's)
- Communication Type: Guidance Document
- Product Type: veterinary
- Office Name: Center for Veterinary Medicine
- Office URL: /offices/center-for-veterinary-medicine/7e30a309-56e4-4e7a-8b8b-e07674bb07b4
- Issue Date: 2006-05-01
- Last Changed: 2019-04-16
- Docket Number: <a href="https://www.regulations.gov/docket/FDA-2000-D-0136">FDA-2000-D-0136</a>

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