Federal (United States) · Regulations
Subpart A — General Information
14 sections
14 sections
- 10 C.F.R. § 35.1Purpose and scope.
- 10 C.F.R. § 35.2Definitions.
- 10 C.F.R. § 35.5Maintenance of records.
- 10 C.F.R. § 35.6Provisions for the protection of human research subjects.
- 10 C.F.R. § 35.7FDA, other Federal, and State requirements.
- 10 C.F.R. § 35.8Information collection requirements: OMB approval.
- 10 C.F.R. § 35.10Implementation.
- 10 C.F.R. § 35.11License required.
- 10 C.F.R. § 35.12Application for license, amendment, or renewal.
- 10 C.F.R. § 35.13License amendments.
- 10 C.F.R. § 35.14Notifications.
- 10 C.F.R. § 35.15Exemptions regarding Type A specific licenses of broad scope.
- 10 C.F.R. § 35.18License issuance.
- 10 C.F.R. § 35.19Specific exemptions.