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# Info Collection on ICH Good Clinical Practice Guide
- URL: https://www.fdaweb.com/info-collection-on-ich-good-clinical-practice-guide/
- Published: 2020-07-23T12:00:00.000Z
- Updated: 2026-09-14T16:22:23.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5147262

*Federal Register* notice: FDA has submitted to OMB an information collection extension for “Guidance for Industry on E6 (R2) Good Clinical Practice; International Council for Harmonization; Integrated Addendum to ICH E6 (R1)” (OMB Control Number 0910-0843). The guidance is intended to help implement improved and more efficient approaches to clinical trial design, including conduct, oversight, recording, and reporting. This is intended to increase clinical trial quality and efficiency while continuing to ensure human subject protection and reliability of trial results. To view the notice, click [here](https://s3.amazonaws.com/public-inspection.federalregister.gov/2020-16036.pdf?ref=fdaweb.com).