42 CFR Subpart D
Additional Submission of Clinical Trial Information
June 11, 2020
§
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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