10 CFR Subpart A
General Information
June 9, 2020
§
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
Tried the LawStack mobile app?
Join thousands and try LawStack mobile for FREE today.
- Carry the law offline, wherever you go.
- Download CFR, USC, rules, and state law to your mobile device.
