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Overview of global clinical data management regulations and standards
2015
Yao xue xue bao = Acta pharmaceutica Sinica
Quality and integrity of clinical trials and associated data management is a basis on the scientific and rightly assessments of drug safety and efficacy. While both normalization and standardization of clinical trial procedures assure quality of clinical trials and the relevant data processes, they will drive and improve the efficiency and reliability of real-world deliverables in clinical trials in turn. Currently, the comprehensive standards and practices of clinical trials and associated
pmid:26911040
fatcat:x5tshjluangkfin6ohhartcr5u