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# Info Collection Extension for GCP Guide
- URL: https://www.fdaweb.com/info-collection-extension-for-gcp-guide/
- Published: 2019-09-06T12:00:00.000Z
- Updated: 2026-09-15T01:48:12.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5144938

*Federal Register* notice: FDA is seeking comments on an information collection extension for “Guidance for Industry on E6 (R2) Good Clinical Practice; International Council for Harmonization; Integrated Addendum to ICH E6 (R1).” The guidance is intended to facilitate implementation of 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 trial results reliability. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2019-09-05/pdf/2019-19113.pdf?ref=fdaweb.com).