Data Integrity in Clinical Trials in [Latest methods]

When: Fri., Nov. 16, 9 a.m.-12 p.m. 2018

Overview: The clinical data recording process, however, as inspected/audited by inspectors/auditors is initiated with the recorded data, either in the Case Report Form, or in some other system, or in an electronic database. Why should you Attend: This course has been planned to provide you with understanding of Principles of Research Data Integrity and the essential skills and tools to evaluate the potential impact of compromised data integrity.

Price: 290

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