Evaluation of Compliance With Legal Requirements Under the FDA Amendments Act of 2007 for Timely Registration of Clinical Trials, Data Verification, Delayed Reporting, and Trial Document Submission.
cross_sectional · Level IV
Where this comes from
- Record sourced from PubMed, PMID 34028509.
- Also identified by DOI 10.1001/jamainternmed.2021.2036 and PMC identifier 8145152.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
This cross-sectional study evaluates clinical trials’ rates of compliance with the legal requirements of the US Food and Drug Administration’s Amendments Act of 2007 for timely registration of clinical trials, data verification, delayed reporting, and trial document submission.
Medical subject headings
- Clinical Trials as Topic
- Guideline Adherence
- Research Design
- United States Food and Drug Administration