Navigate the pathway to Canadian market approval with confidence through our expert technical file compilation and gap analysis service for medical devices. Our service is meticulously designed to simplify the complex regulatory landscape of Health Canada, ensuring your medical device meets all compliance standards for a successful market entry, without the stress or complications typically involved.
Understanding the nuances of the Medical Devices Regulations (SOR/98-282) under the Food and Drugs Act, our team focuses on the critical requirements for your technical file. From the initial concept to the finished product, we evaluate your device against these stringent regulations, identifying any compliance gaps and offering comprehensive support to address them efficiently.
Our service goes beyond just identifying gaps; we provide holistic support to fill them. If your documentation is missing key elements such as biological or clinical evaluations, we stand ready to assist. Our expertise includes:
Designed for both innovators and manufacturers, our service aims to streamline your journey to the Canadian market, making regulatory compliance an achievable milestone rather than a daunting obstacle. Partner with us to ensure that every aspect of your medical device, including those initially overlooked, is meticulously addressed, paving the way for a successful launch that contributes to health and well-being across Canada.
We support in setting up a compliant and robust technical file that fulfills all requirements of the SOR/98-282. You have already a technical file but needs an update? We are here to help.
You have difficulties to identify which documentation is required for your device classification? Leave it with us. Our experts will guide step by step.
Your product is already on the market. Do you know which post market requirements need to be met? Don’t worry. We support with the proper planning and define the most appropriate post market reporting. This ensures your technical file will stay up-to-date.
