Innovations In E-Consent: Reducing Regulatory Risk While Improving Participant Comprehension

Informed consent has a major impact on regulatory compliance, enrollment rates and expenses across the life of your study. Yet the traditional paper-based process has transformed informed consent into one of the most cited deficiencies.

Regulatory agencies and the world’s leading biopharmaceutical companies have been pushing for a more effective informed consent process - and the technology has finally arrived.

Watch this on-demand webinar to find out about groundbreaking new innovations in electronic informed consent (e-Consent), and learn how you can use e-Consent in your trials to increase participant compliance, retention and comprehension while reducing regulatory risk.