eConsent can reduce barriers and improve the clinical trial experience for patients and sites. We sat down with Dr Caroline Forkin, senior director medical affairs of FIRECREST, ICON, to discuss this ...

Electronic informed consent (eConsent) tools are emerging as a valuable solution in the quest to deliver a more patient-centric clinical trial experience. eConsent platforms take the complex paper ...

In a webinar scheduled for April 16 at 1pm ET, Aneesh Chopra, who served as the first Chief Technology Officer during the Obama administration and serves as president of CareJourney, will moderate a ...

In my many years leading participant recruitment in health research, one of the most common questions I’m asked is, “How do you enable eConsent for health research?” Having led recruitment for a large ...

One of the major obstacles for researchers when deciding whether to adopt an eConsent approach within their study has been a lack of understanding surrounding regulatory support. While many would ...

Post-hoc analyses of a large, randomized clinical trial have revealed the potential advantages associated with electronic informed consent (eConsent) in acute ischemic stroke studies, including ...

Over 70% of potential research participants live >2 hours away from a research site, & patient drop-out rates can reach 30% depending on the therapeutic area. The Solution: Medable eConsent Why? 1.

For those suffering from rare and intractable diseases, clinical trials represent hope – for a more effective treatment, for a cure, or to help future patients facing similar challenges. Facilitating ...

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