Learn More
Log In
Sign Up
General Information | Midpage
Collections
Code of Federal Regulations
Title 10
Chapter I
Part 35
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
Exemptions regarding Type A specific licenses of broad scope.
35.18
License issuance.
35.19
Specific exemptions.