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Code of Federal Regulations
C.F.R. Title 42—Public Health
CHAPTER I—PUBLIC HEALTH SERVICE, DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER A—GENERAL PROVISIONS
PART 11—CLINICAL TRIALS REGISTRATION AND RESULTS INFORMATION SUBMISSION
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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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