10 CFR Part 35 - Subpart A - General Information
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- § 35.1 Purpose and scope.
- § 35.2 Definitions.
- § 35.5 Maintenance of records.
- § 35.6 Provisions for the protection of human research subjects.
- § 35.7 FDA, other Federal, and State requirements.
- § 35.8 Information collection requirements: OMB approval.
- § 35.10 Implementation.
- § 35.11 License required.
- § 35.12 Application for license, amendment, or renewal.
- § 35.13 License amendments.
- § 35.14 Notifications.
- § 35.15 Exemptions regarding Type A specific licenses of broad scope.
- § 35.18 License issuance.
- § 35.19 Specific exemptions.