Subpart A—General Information

1. CFR
2. ›
3. Title 10
4. ›
5. Chapter I
6. ›
7. Part 35
8. ›
9. Subpart A

Sections

Section numbering in the official eCFR can be non-consecutive. Omitted section numbers are not treated here as reserved unless the source explicitly labels them that way.

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