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# Info Collections Consolidated for Informed Consent/IRBs
- URL: https://www.fdaweb.com/info-collections-consolidated-for-informed-consent-irbs/
- Published: 2019-08-14T12:00:00.000Z
- Updated: 2026-09-15T01:43:55.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5144766

*Federal Register* notice: FDA is seeking comments on an information collection revision for “Protection of Human Subjects; Informed Consent; and Institutional Review Boards (IRB) — 21 CFR Parts 50 and 56” (OMB Control Numbers 0910-0755 and 0910-0130). On its own in initiative, the agency is consolidating the information collections pertaining to human subject protection and IRB responsibilities. FDA says the consolidation will improve its operational efficiency. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2019-08-14/pdf/2019-17462.pdf?ref=fdaweb.com).