Federal (United States) · Regulations
Subpart B — Registration
5 sections
5 sections
- 42 C.F.R. § 11.20Who must submit clinical trial registration information?
- 42 C.F.R. § 11.22Which applicable clinical trials must be registered?
- 42 C.F.R. § 11.24When must clinical trial registration information be submitted?
- 42 C.F.R. § 11.28What constitutes clinical trial registration information?
- 42 C.F.R. § 11.35By when will the NIH Director post clinical trial registration information submitted under § 11.28?