In Part 3 of the Webinar “How Research Sites Can Win With Decentralized Trials” the panelists cover questions about eConsent such as:
- Are sites really prepared to eConsent participants?
- How to ensure the patient is truly informed?
- How to make sure the remote consent conversation is compliant with regulations about confidentiality?
- How to avoid overwhelming potential participants while preserving the thorough consent process?
- How to account for cultural not just language barriers?
- Why sites need to own the informed consent process as well as maintain a conversation with the sponsor?
- What is the real problem with informed consent that the industry already had pre-Covid? And how can we address it?
Are you planning to incorporate virtual modalities in your trial? Finding vendors can be a real challenge. Check out The Ultimate Guide to Virtual Trial Vendors (bit.ly/30SkSiw) to find the best partners for your virtual/hybrid clinical trial and support your patients and operations remotely.