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U.S. Code of Federal Regulations
Regulations most recently checked for updates: Sep 16, 2025
All Titles
Title 42
Chapter I
Part 11
Subpart D - Subpart D—Additional Submission of Clinical Trial Information
§ 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?
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