SUBPART A—General Information (§35.1 to §35.19)
- 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.