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Additional Submission of Clinical Trial Information | Midpage
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Code of Federal Regulations
Title 42
Chapter I
Subchapter A
Part 11
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?