Nordic CRO Larix signs Master Service Agreement with Viedoc
Nordic full-service CRO Larix has signed a master service agreement with Viedoc and will soon initiate the first clinical study powered by the Viedoc EDC system.
“Viedoc’s big selling points are their streamlined setup process and a highly user-friendly interface. That’s exactly what our small- and middle-sized clients in the biotech industry are looking for in an EDC system,” says Lisa Thell, Director Data Management at Larix.
Lisa Thell, Director Data Management at Larix.
Larix works with several different EDC systems depending on the client and study at hand.
“With Viedoc, we get an EDC system which allows our clients to focus entirely on their research, instead of spending large amounts of time on lengthy setup processes and learning how to manage the system. We want the best solution for every given study when offering an EDC solution to our clients.”
“We’re excited to start working with Larix and get the first study underway. Our goal from the start has been to make electronic data capture smarter, faster and easier than ever before – so it’s rewarding that Larix has chosen our system based on those exact factors,” says Henrik Blombergsson, COO and co-founder Viedoc.
Larix is a family founded, privately-owned CRO offering solutions in statistics, data management, clinical operations, medical writing, pharmacovigilance and data monitoring committees. Larix was founded in 2001 by Klaus Juel Olsen. In 2003, the company expanded with services within data management, and additional statisticians were employed. The clinical research service was added in 2008, simultaneously with an independent QA function. In 2010 the services were broadened to include pharmacovigilance. In 2015 Larix expanded to Sweden, Norway and Finland and as next step the Swedish office is now moving into Medicon Village in Lund.
Viedoc is a modern and future-proof EDC system that allows clinical trial sponsors and study sites to easily and securely collect, validate, transmit and analyze clinical study data. A proven software since 2003 which meets or surpasses all regulatory benchmarks. Designed to be as intuitive as possible, Viedoc saves time and frustration from users at every level, allowing clinical trial organizations to have more focus on their own innovation and leadership. www.viedoc.com