Regulatory roadmap for biotech startups in Canada What you'll find in this document In Canada, what is considered a “Medical Device”?Regulatory approval processPre-market approval (MDL)Medical Device Establishment License (MDEL)Clinical trialsPost-market surveillance Fill out the form to access your comprehensive guide Please enable JavaScript in your browser to complete this form.Name *FirstLast Name Email select Email *CompanyPlease select *By submitting this form, you consent to the collection and use of your information for the purposes outlined in our privacy policy.Download