One of the critical parts to improving patient engagement in the clinical trials is improving the informed consent process
This webinar recording explores 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.
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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.
Key insights include:
- Learn how to reduce barriers to participation for sites and patients
- Discover the advantages to sponsors and sites in ensuring compliance with the informed consent process
- Explore the current regulatory guidance and geographical differences
- Examine the latest TransCelerate eConsent landscaping findings