# Frequently Asked Questions - IRB Registration: Guidance for Institutional Review Boards (IRBs) - FDA Guidance Document Source: https://www.globalkeysolutions.net/guidances/guidance-document/frequently-asked-questions-irb-registration-guidance-for-institutional-review-boards-irbs/7a3de4e3-164a-476e-983c-437126be73f7 > FDA guidance document: Frequently Asked Questions - IRB Registration: Guidance for Institutional Review Boards (IRBs). Issue date: July 09, 2009. Get complete insights and analysis. --- ## Details - Title: Frequently Asked Questions - IRB Registration: Guidance for Institutional Review Boards (IRBs) - Communication Type: Guidance Document - Product Type: devices - Office Name: Office of the Commissioner - Office URL: /offices/office-of-the-commissioner/79483979-9582-427f-ac3d-46c715811424 - Issue Date: 2009-07-09 - Last Changed: 2021-07-21 - Docket Number: FDA-2009-D-0312 ## Related Documents - [Process for Handling Referrals to FDA Under 21 CFR 5054 - Additional Safeguards for Children in Clinical Investigations: Guidance for Clinical Investigators, Institutional Review Boards and Sponsors](https://www.globalkeysolutions.net/guidances/guidance-document/process-for-handling-referrals-to-fda-under-21-cfr-5054-additional-safeguards-for-children-in-clinical-investigations-guidance-for-clinical-investigators-institutional-review-boards-and-sponsors/57b4b090-bd0e-4212-a631-6ebc41223136) - [180-Day Exclusivity When Multiple ANDAs Are Submitted on the Same Day](https://www.globalkeysolutions.net/guidances/guidance-document/180-day-exclusivity-when-multiple-andas-are-submitted-on-the-same-day/26a43ba4-c062-4358-b394-9623fa7f9f78) - [Data Retention When Subjects Withdraw from FDA-Regulated Clinical Trials: Guidance for Sponsors, Clinical Investigators, and IRBs](https://www.globalkeysolutions.net/guidances/guidance-document/data-retention-when-subjects-withdraw-from-fda-regulated-clinical-trials-guidance-for-sponsors-clinical-investigators-and-irbs/3358ed6a-403d-4aaa-b66c-941d2d2630ab)