42 CFR 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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