Federal (United States) · Regulations
Subpart A — General Provisions
5 sections
5 sections
- 42 C.F.R. § 11.2What is the purpose of this part?
- 42 C.F.R. § 11.4To whom does this part apply?
- 42 C.F.R. § 11.6What are the requirements for the submission of truthful information?
- 42 C.F.R. § 11.8In what format must clinical trial information be submitted?
- 42 C.F.R. § 11.10What definitions apply to this part?