Innovative Technology Solutions for Implementation of ICH E6(R2)

Sponsors running clinical research studies face enormous pressures today. From complex study designs, industry cost constraints, new geographical locations and significant technological advancements, there are many challenges to address. The International Council for Harmonization (ICH) efficacy guideline on Good Clinical Practice (GCP) aims to help sponsors keep up with these major shifts and implement improved practices in the industry. In this webinar, we discuss how the ICH has changed with the recently approved revision E6(R2) and outlines some of the major areas where sponsors can develop more efficient approaches in the design and conduct of their clinical trials. Learn how to better utilize your data to mitigate risk while also complying with the new ICH GCP E6 Revision 2 guidelines. Enable your entire study team to create, view and manage issues that emerge during the execution of a trial in real time.