Code of Federal Regulations · Subpart

Subpart D — Additional Submission Of Clinical Trial Information

42 C.F.R. pt. 11, subpt. D

• § 11.60 What Requirements Apply To The Voluntary Submission Of Clinical Trial Information For Clinical Trials Of Fda-regulated Drug Products (including Biological Products) And Device Products?
• § 11.62 What Requirements Apply To Applicable Clinical Trials For Which Submission Of Clinical Trial Information Has Been Determined By The Director To Be Necessary To Protect The Public Health?
• § 11.64 When Must Clinical Trial Information Submitted To Clinicaltrials.gov Be Updated Or Corrected?