If you are thinking about bringing a healthcare technology to market, it is essential that you establish your regulatory pathway from day one!
H2i is supporting an upcoming workshop series focused on essential regulatory, clinical, and quality requirements for bringing new health care technologies to market. The goal of the workshop series is to provide participants with an understanding of the necessary processes, data, timelines and costs that are directly associated with securing market authorization within the US, EU and Canadian regulatory jurisdictions.
The workshop series includes the following 3 modules conducted by our team of experts (see below):
Wednesday Jan 31, 2018: Product classification and regulatory pathways in the US, EU, and Canada
Wednesday March 7, 2018: Developing a regulatory strategy from product concept through to market authorization application
Wednesday April 25, 2018: Executing a regulatory strategy towards market authorization
Each module will run from 4:00 PM to 8:00 PM at ONramp RBC innovation hub @ 100 College St in the Banting Institute
There are only 50 available spots so registration will be on a first come first serve basis and is looking for your commitment to all 3 sessions.