Institutional Review Boards

This practice note discusses Institutional Review Boards (IRBs) within the United States, including their purpose, history, and regulatory framework. The note is a valuable resource for advising life sciences and healthcare clients on IRB-related matters and ensuring compliance with federal regulations and ethical standards.  

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Related Content

• Institutional Review Board (IRB) Formation, Organization, and Operation Checklist
  Use this checklist to guide you through legal and compliance considerations related to the formation, organization, and operation of an IRB.

• Clinical Trials Resource Kit
  Find information about key concepts and considerations related to setting up and managing human subjects research and clinical trials for drugs and medical devices.

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