Ease the burden on your sites and make it easier and more appealing for patients to enroll and remain engaged.
This unique interactive forum provides the opportunity to strategize with your peers, partners, and providers, and leverage the expertise of renowned industry leaders from companies of all sizes as we work together to improve oversight and achieve a confident state of inspection readiness.
Taking a Risk-Based Approach to Quality: It Doesn't Have to be Spooky
Tuesday, October 25th, 2022 9:30 am - 10:00am EST
It may feel safer to shine the quality flashlight on every document before it gets filed in the Trial Master File (TMF), but do these oversight practices end up leaving more of the scariest risks in the dark? With the Great Resignation hitting clinical trials hard, it's more important than ever to apply the appropriate level of resources to activities that have the most impact. Explore how you can facilitate a risk-based approach to quality processes and documentation:
Ease the burden on your sites and make it easier and more appealing for patients to enroll and remain engaged.
Increase transparency, improve communications and reduce administrative burden for all clinical trial stakeholders.
Manage trial master files from planning through archive with solutions designed to improve workflow efficiency, promote collaboration, and support compliance.