Rather than the costly practice of frequently flying monitors to each site in your multicenter clinical trial, access digital subject binders for data verification with our easy-to-use web application built specifically for remote and risk-based monitoring. Additionally, push regulatory binders to sites in just a click.
No more finding desk space and documents for visiting monitors, no more wondering where to file something that belongs under multiple binder tabs or proactive checking for expiring documents, and no more 3-ring binders! SourceDrive understands your workflows, eliminating the busy work that is holding your site back.
SourceDrive is fully compliant with 21 CFR Part 11 and HIPAA.
All data is kept and redundantly backed-up in a cloud hosting environment that is secured by rigorous
administrative, physical, and technical safeguards.
Chief Executive Officer
Chief Product Officer
Chief Technology Officer
VP of Engineering
We have a well-balanced founding team with clinical and regulatory expertise and a combined 20 years experience building life sciences enterprise software. Previous to Invio, we’ve worked at Fred Hutch, Olympus Medical Devices, Epic, Appature, and IMS Health among others.
Our goal is to advance the speed and quality of medical innovations for everyone.