Subpart A. Subpart A—General Information
- § 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 -
- § 35.18 - License issuance.
- § 35.19 - Specific exemptions.