Members benefit from being part of C-OPN by:
- Having access to necessary C-OPN resources to facilitate the execution of a research project including: the registry, the de-identified database (including demographic, clinical, and neuropsychological information as well as imaging) via the C-OPN LORIS platform (https://copn.loris.ca/), and the biobank (including biological materials such as blood) in accordance with the C-OPN Data Sharing Policies
- Check out the exciting research projects already leveraging C-OPN resources by clicking here
- The right to submit an item on the Executive Committee’s agenda for discussion
- The ability to attend the General Assembly
- Be part of a national network of Parkinson’s research and receive updates or opportunities related to C-OPN