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Biobank for Translational Medicine: Standard Operating Procedures for Optimal Sample Management
Published on: November 30, 2022
[The handling and using of medical research data]
O G Melikhov1, S M Lukerin2, A B Zudin3
1The Society with Limited Liability "The Institute of Clinical Research", 119590, Moscow, Russia, melikhov.oleg@gmail.com.
Abstract:
The results of scientific research can be trusted when initial data is processed properly. To watch out quality of data is the most important in those research studies that provide their results to Russian health care officials for management decision-making that effect medical care support on national scale. The financial support of science within the framework of public contracts turns out less efficient when deductions are based on unreliably collected, altered or omitted information. When electronic systems are applied in data collection, they are to meet definite requirements. There are several international documents defining requirements to electronic systems collecting and processing information in medical scientific research. In the Russian Federation, such requirements are absent. The solution of this problem is in gradual implementation of common international standards into practice of collecting research data initially through researchers' training and then through Russian regulatory documentation amendment.
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