With the release of ICH E6(R3), expectations around quality, flexibility, and data integrity have evolved—placing greater emphasis on risk-based approaches, patient-centricity, and digital enablement.
This refresher course is designed for clinical research professionals who have completed the foundational training, Ethics and Human Subject Protection: An Introduction with ICH E6(R3) Guidance.
Now updated to reflect the latest guidance from ICH E6(R3), this on-demand training is a must for clinical research professionals at any stage of their career—whether you’re just starting out or looking to reinforce your foundational knowledge.
This session dove into alternative resourcing models and funding strategies designed to stretch limited resources without sacrificing quality or compliance. Experts highlighted opportunities for sites and sponsors to collaborate on centralized qualification, creative contracting approaches, and shared training and infrastructure support.
This webinar provided practical guidance on optimizing system setup, consolidating processes for greater efficiency, and scaling technology to save time, money, and resources. Participants heard tips on partnering with vendors for training, validation, and best-practice support, while also learning how to advocate for collaborative data sharing across site and sponsor workflows.