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Regulacje i polityka gospodarcza · 21/09/2016

FDA Final Rule Details Requirements for Clinical Trials Registration and Results Submission

The FDA has released a final rule outlining the requirements for submitting clinical trials registration and results information, including adverse event data, to ClinicalTrials.gov, a database operated by the National Library of Medicine, to enhance clinical trial design, patient eligibility, and public trust in clinical research.

Source: Federal Register — All DocumentsOpen original release →