§11.20. Who must submit clinical trial registration information?
42 C.F.R. § 11.20
The responsible party for an applicable clinical trial specified in § 11.22 must submit clinical trial registration information for that clinical trial.
Notes, amendments, and revision history
Authority
Authority: 42 U.S.C. 282(i); 42 U.S.C. 282(j); 5 U.S.C. 301; 42 U.S.C. 286(a); 42 U.S.C. 241(a); 42 U.S.C. 216(b).
Source
Source: 81 FR 65138, Sept. 21, 2016, unless otherwise noted.