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Regulations21 CFR 812 - Investigational
Device Exemptions 21 CFR 50 - Protection of Human
Subjects 21 CFR 56 - Institutional Review
Boards 21 CFR 54 - Financial Disclosure
by Clinical Investigators 21 CFR 58 - Good Laboratory Practice
for Nonclinical Laboratory Studies 21 CFR 820 - Quality System Regulation Last modified date 01/02/2002 |
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Center for Devices and Radiological Health / CDRH