ISO Standards, MDSAP, and Health Canada Regs
Hi all. I’m currently in the process of developing a medical device in Canada and I’m trying to put together a roadmap of sorts so I can understand the process of bringing a device to market.
I’m brand new to the industry and don’t really know what I don’t know. I would love to pick the brain of someone who’s done it all before.
I appreciate any advice on educational resources, industry organizations to join, direct contacts to reach out to, conferences to attend, etc. or just any advice you may have.
Edit: the device is a class II drape made mostly of transparent plastic.