FDA-HUMANITARIAN DEV › Historical Revision Information
Guidance for HDE Holders, Institutional Review Boards (IRBs), Clinical Investigators, and FDA Staff - Humanitarian Device Exemption (HDE) Regulation: Questions and Answers
Guidance for HDE Holders, Institutional Review Boards (IRBs), Clinical Investigators, and FDA Staff - Humanitarian Device Exemption (HDE) Regulation: Questions and Answers
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Document Number
FDA-HUMANITARIAN DEV
Revision Level
2001 EDITION
Status
Superseded
Publication Date
July 12, 2001
Page Count
9 pages