Toronto, Canada (PRWEB) March 07, 2014
This webinar will provide a regulatory perspective on what is expected from an independent and objective assessment of clinical data. Join esteemed speakers Marc Buyse, Founder of IDDI and CluePoints, and Francois Torche, CEO of CluePoints, as they discuss:
- What the EMA and FDA are encouraging sponsors to look at as part of their assessment of data quality
- Identifying the different types of data analysis required to de-risk your study
- A review of case studies that exemplify a powerful, holistic approach to data assessment
For more information on this webinar or to register, visit Risk-Based Monitoring & Central Statistical Monitoring.
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