WHO clinical registry standards?
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Interventions from clinical trials are a crucial component of healthcare. “Every clinical study must be recorded in a publicly accessible database before recruitment of the first subject,” the Declaration of Helsinki mandates. Establish a clinical registry to create a baseline data quality level, validate data, and improve universal access and Validity of research data. A clinical trial register is an official record of the clinical research’s minimal, globally agreed-upon quantity of data that is kept and maintained in a database.
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