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.