Digital vs digitized: Common myths about eConsent for clinical trials

Alex Burrington, CTI Principal of Vertex, and Andrew Mckinnon, VP, GM of eConsent discuss common myths around eConsent, how to improve comprehension with patient-centric consent, and how to use a digital consent management tool to improve trial compliance, quality, and oversight.

Blog posts

Clinician Reported Outcomes (CROs): A universal approach

6 min

Get the basics on ClinROs, why they are important, the industry governance around them, and how their electronic versions can benefit clinical trials.

See how Medable can make your trials more efficient.