Resource Library

In this webinar, we 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.

Gain guidance on misconceptions around the cost-effectiveness of electronic patient-reported outcomes (ePRO) and key points to consider when evaluating ePRO.

Collecting participant data securely is a critical part of running any clinical trial, whether it is decentralized, in-clinic, or somewhere in between. Medrio EDC and ePRO solutions are important assets that help CROs and sponsors do more with less.

Participant education is a critical part of informed consent and one that is easy to improve by leveraging established patient education best practices. Medrio CEO Nicole Latimer discusses some of the most successful approaches she has seen in her career:

Many early phase studies rely on manual methods of managing participant randomization and the study supply chain. But increasing complexities in both study design and global supply chain necessitate more flexible, responsive solutions for early phase studies, in particular. 

Does your CRO or sponsor have a policy around IP numbering in clinical trials? If not, they could be putting your clinical trial at risk.