Data Management Services
- Categories:Clinical Trials
- Time of issue:2021-03-25 14:57:13
The quality of clinical trial data is the basis for evaluating the results of clinical trials. The accuracy and correctness of the data are extremely important to ensure the quality of clinical trials, so great attention must be paid to traceability. Data management should be carried out carefully to ensure the accuracy and correctness of the trial’s data.
Clinical trial data management requires the joint efforts and collaboration of clinical trial research project teams.
The personnel involved in CRCS clinical trial data management include:
➣ Sponsor: the ultimate responsible person for the quality of clinical data → audit
➣ Researcher: ensure that the data report is accurate, complete and timely → traceability
➣ Inspector: review the data on CRF according to the source document → correctness and completeness
➣ Data administrator: participate in the design of CRF and logical inspection → Data query form
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