Federal Regulations

DOE requires compliance with all applicable Federal requirements for the protection of human research subjects, including the Department of Health and Human Services Office for Human Research Protections Requirements

All DOE-funded and conducted studies must comply with both:
a) 10 Code of Federal Regulations (CFR) Part 745 (DOE’s implementation of 45 CFR Part 46, Subpart A (implemented by DOE as 10 CFR Part 745):  Research initiated prior to January 19, 2019 must comply with the Pre-2018 Requirements, and research after this date must comply with the 2018 Requirements.
b) 45 CFR Part 46 (all other subparts, as they relate to the study).
Food and Drug Administration Requirements (for Drug and Device-Related Studies Under FDA’s Purview)
a) 21 CFR Part 50, Protection of Human Subjects
b) 21 CFR Part 56, CFR - Institutional Review Boards
c) 21 CFR Part 812, Investigational Device Exemptions
d) 21 CFR Part 312 Investigational New Drug Application
e) 21 CFR Part 600, Biologic Materials
f) 21 CFR Part 361, Prescription Drugs
g) 21 CFR Part 54, Financial Disclosure
h) 21 CFR Part 58, Good Laboratory Practices