Event Date: Dec 07, 2017
One of the critical parts to improving patient engagement in the clinical trials is improving the informed consent process.
eConsent has the potential to transform the conventional informed consent approach in clinical trials in a truly patient-centric way, while enhancing the consenting process for all stakeholders involved. From reducing errors and the burden on site staff to improving the patient experience, eConsent can significantly impact a study.
This webinar will explore the latest industry and regulatory developments relating to the use of eConsent in clinical trials and what sponsors and sites need to consider before they deploy this in clinical trials.
Click here for additional information and registration details.
