Stuart Cotter

Review a list of considerations for site-sponsor tasks to streamline startup, reduce redundancy, and refine technology choices for effective partnerships.

Global & FDA regulations dictate how researchers organize & store trial documents. Learn the basics of eTMF & eISF clinical research tools

Explore the benefits of pre-screening potential participants before they move on to the informed consent process.

The Bring Your Own Technology philosophy will produce synchronization between sites & sponsors, which improves both care & clinical outcomes.

If presented with a new study, are you prepared to take it on? Efficient study activation can set the pace for a successful clinical trial.

Advarra eRegulatory Management System now supports the storage and remote monitoring of Subject Binders and SOPs, increasing compliance, and centralizing your study documents.

Using physical binders or an internal shared drive can slow research operations. Implementing an eRegulatory system helps institutions streamline research by transforming key workflows.

Advarra's experts answer audience questions from our Regulatory Fine Points: Exploring 21 CFR Part 11 Validation webinar.