EDC
Clinical trials are complex and time-consuming, but using your EDC shouldn't be. You need a reliable, central hub that maximizes your efficiencies and allows you to reach your goals sooner—all while tightening up your costs and giving you full control over your clinical trial research.
ePRO
Your ticket to faster insights from patient-reported data, more control over timelines, and improved patient engagement.
Decentralized and Hybrid Trials
The benefits to your patients and your team are plentiful. Removing the patient burden of always coming into the clinic increases recruitment, compliance, and patient engagement.
eConsent
Medrio’s eConsent solution empowers organizations to accelerate all aspects of the consent process, from setting up and modifying forms to ensuring patient comprehension, while remaining in full regulatory compliance.
Heron Therapeutics Speeds Up Database Creation with Medrio EDC
San Diego-based biotech trusts Medrio EDC for Data Collection. From drag-and-drop features to outstanding support, Medrio offers simplicity without compromise.
Facts and Misconceptions about ePRO Cost-Effectiveness
Gain guidance on misconceptions around the cost-effectiveness of electronic patient-reported outcomes (ePRO) and key points to consider when evaluating ePRO.
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Designing ePRO and eConsent Solutions that Participants and Sites Want
In this webinar, Medrio Subject Matter Experts 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.
Start with 'Why' When Adopting New Tech to Support Hybrid Decentralized Trials
Sponsors can reduce the burden of adopting new hybrid decentralized trial technology by explaining its relevance and taking steps to reduce the cost of change.
