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# Petition Seeks GMP Amendment for Sampling Logbooks
- URL: https://www.fdaweb.com/petition-seeks-gmp-amendment-for-sampling-logbooks/
- Published: 2025-04-16T12:00:00.000Z
- Updated: 2026-09-14T15:09:40.000Z
- Author: David McFarland
- Tags: Drugs, #legacy-id-D5159020

A new [citizen petition](https://downloads.regulations.gov/FDA-2025-P-1086-0001/attachment%5F2.pdf?ref=fdaweb.com) is asking FDA to amend the requirements under 21 CFR Part 211 (current good manufacturing practice for finished pharmaceuticals) to mandate the use of separate sampling logbooks or equivalent electronic logs for all sampling activities, including raw materials, in-process materials, finished products, and stability samples.