2023 - A Step-by-Step Approach to eSource in Clinical Trials

The shift from manual data entry of medical records to the automatic acquisition of data from multiple real-world sources is no longer a ‘nice to have’ in clinical trials. In our post-pandemic landscape, sponsors embracing eSource realize key competitive advantages:
Increased early access to a steady stream of data for decision-making
Compressed trial timelines
Reduced burden on trial sites and patients
However, change is hard, especially at scale. Challenges persist around change management, regulatory compliance, trial complexity, data quality and technology implementation. Leading sponsors are adopting a strategic, step-by-step approach that minimizes disruption and risk while maximizing a positive return right from the start.
Join this webinar to learn how to get started with a focus on early wins to realize long-term success with eSource and real-world data across traditional, decentralized, virtual and digital-first clinical trials.