EP 1: Coordinated Registry Network

 

The coordinated registry network (CRN) aims to collect and compare data from diverse registries with similar data points, to help physicians address specific questions based on collective real-world data.

Steve Elias meets with Jens Eldruip-Jorgensen (Maine, US), Marlin Schul (Indiana , US) and Nicholas Osbourne (Michigan, US) to find out more about the aims of the Coordinated Research Network and its impact on real-world practice to treat patients with venous disease. Highlights include discussions around the benefits and challenges of registry data, as well as a look at the current data coming out from the CRN and its implications for clinicians.

Submit your question to Steve via: podcast@radciffe-group.com. Hosted by [inert Steve Twitter]. Produced by @RadcliffeVASCU.