Melissa May
Melissa May is a Subject Matter Expert in Life Sciences at Acolad, specializing in Clinical and Biopharma. With 19 years of experience in the language services industry, she has focused on ensuring compliance, accuracy, and accessibility in global clinical trials.
Successfully Implementing eConsent for Multilingual Clinical Trials
For clinical trials involving linguistically and culturally diverse patient populations, successful eConsent implementation goes beyond simply digitizing consent forms. A successful implementation strategy includes regulatory compliance, data privacy, and cultural sensitivity.