Onboarding with CRIO's Clinical Trial Software: A Real-Life Experience from a Research Site

Are you interested in investing in clinical trial software at your research site, but worried how your staff will adapt to the change? At Team CRIO, we partner with many sites who experience this challenge; that’s why we ensure you’ll have a dedicated project manager for your team.

In this webinar, Luke Snedaker, the VP of Clinical Research at Lucas Research, goes through the process & challenges of onboarding with CRIO’s eSource, CTMS, and eRegulatory software. Get an exclusive peek into how the Lucas Research staff adopted CRIO, and how you can, too.

Ask Me Anything – Tools for Top Performing Sites

Kristen Bosse, Director of Product Development, is CRIO’s in-house product guru. In this Ask Me Anything, a CRIO expert roundup, Kristen discusses CRIO’s products, UX design and beta testing, and shares recommendations for sponsors looking to identify the best sites for their trials. What differentiates CRIO’s products from any other products on the market? We...

Unlocking the Benefits of CRIO: eSource & eConsent

eConsent: The Benefits With the recent push toward Decentralized Clinical Trials, many sponsors are adopting eConsent. eConsent allows patients to consent electronically, whether in clinic or remotely, from the convenience of their home. eConsent offers sponsors, CROs investigators and patients these benefits: Removal of errors by ensuring completion of all fields Accuracy of date-times through...

Data Blast from the Past: From Triplicate to eCRF

Jonathan Andrus, President & COO at CRIO, is an active thought-leader and presenter in the life sciences industry. He serves on the board and executive committee of the Society for Clinical Data Management (SCDM) and is co-lead with the Decentralized Trials and Research Alliance (DTRA) workstream initiative. The year was 1996 – the year that...