-
Clinical Risk Based Monitoring
Incorporating a Fully Operational Risk Based Monitoring Structure to Achieve Greater Trial Performance
5-6 Dec 2017
Philadelphia, PA, United States of America
- Why You Should Attend
-
Clinical Risk Based Monitoring
As biopharmaceutical companies continue to retain a reliance on data analytics, they possess an increase capability to actively assess and continuously monitor trial sites, overall quality and patient safety, as well as outcomes. Risk-based monitoring is now the industry standard to achieve safer and improved trial outcomes which is now leading organizations in the industry to proactively examine how to effectively incorporate and transform into a fully operational RBM trial structure.
This premier marcus evans event will bring together the foremost leaders in Risk Based Monitoring, Clinical QMS, Clinical Safety and Clinical Trial Management to explore ways to reduce costs while enhancing overall trial quality, data, and outcomes through a more risk based approach.