Designing ePRO and eConsent Solutions that Participants and Sites Want

Participant-focused eClinical technologies offer significant potential to decrease paper-based processes and improve end-user experiences in collecting patient-reported outcomes (PRO) and informed consent, but many users continue to experience rigid technology, complicated hardware provisioning processes, and clunky implementations that leave sponsors, CROs and sites questioning the value. 

In this webinar, Melissa Newara, Senior Director of Subject Matter Expertise at Medrio, and Tina Caruana, Subject Matter Expert – eClinical Solutions at Medrio will explore the powerful way that ePRO and eConsent tools, when implemented effectively, can enhance the participant experience and improve compliance while reducing the burden on site staff. Learn how the right eClinical technologies close gaps in data accuracy, reduce context switching, and enable closer communication between participants and study professionals. 

They will also review how today’s patient-centered technologies can flex to meet the needs of each unique protocol design – whether onsite, at-home, hybrid, or fully decentralized. 

You’ll learn:

• How to identify solutions that are purpose-built for participant convenience and ease of use
• Ways ePRO and eConsent solutions reduce site burden
• Best practices for implementing patient-centered technologies in your organization 
• Truths and misconceptions about the actual cost of today’s ePRO and eConsent technologies