
Why Paper Consent is a Bottleneck in Your Clinical Trials – and How Executives are Transforming Burdens into Efficiencies
Learn how a modern Consent solution can help you unify the informed consent process with eCOA, accelerating study startup and removing eCOA from the critical path. In this on-demand webinar, Medidata experts share key operational and technology strategies for reducing site burden, ensuring compliance, and maximizing flexibility for trials of any type or scale—from simple designs to complex pediatric and multi-arm studies.