Code of Federal Regulations · Subpart
Subpart A — General Information
10 C.F.R. pt. 35, subpt. A
- § 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