Mastering eConsent: 3 Proven Implementation And Adoption Best Practices

By Tina Caruana, eClinical Solutions Subject Matter Expert at Medrio

Implementing electronic consent offers numerous advantages for sponsors, CROs, sites, and participants, but ensuring a seamless and enduring transition requires proper implementation processes and ongoing support. The introduction of new technologies and processes can be overwhelming for research site staff, particularly when it comes to the critical aspect of informed consent in a trial's success. A poorly executed implementation may even elevate the risk of sites reverting to traditional paper processes.

Drawing from lessons learned in various eConsent implementations, we advocate three essential best practices to facilitate a smooth and sustained transition: fostering collaboration among sites, ensuring IRB/IEC preparedness, and providing comprehensive training for both sponsor/CRO staff and investigator sites. By incorporating these practices, stakeholders can navigate the complexities of eConsent adoption with confidence and enhance the overall efficiency and success of clinical trials.