The video below shows TRI’s CIO Chad Finch introducing the webinar:
This webinar is free to attend for anyone who is directly involved in the planning and execution of clinical trials.
WHO SHOULD ATTEND?
Anyone who is already running clinical trials using the principles of quality management as defined by ICH E6 (R2) and risk-based monitoring, or anyone who plans to do so in the near future.
Anyone with a general interest in R2 compliance, or in the process of looking at how they may use technology to support them with R2 compliance and risk-based monitoring.
WHY ARE WE RUNNING THIS EVENT?
With ICH E6 (R2) now approved, and adoption by the EMA already scheduled for June this year, technology is going to play a big part in both enabling R2 compliance and providing the evidence required to prove compliance. TRI are actively engaged in supporting many companies with their preparation for R2 compliance and are always looking for ways to help guide industry as to how to best approach the challenges and opportunities that compliance can present. This webinar will give us the opportunity to share some of our experiences of working with other companies and help you plan your route to compliance.
HOW TO REGISTER
Simply click on the link below to register for the free webinar: