Navigating Regulatory and Quality Pathways in Canadian Medtech: Foundations, Advocacy, and Industry Impact
Are you new to the regulatory and quality fields in medical technology, or seeking clarity on how to engage with government and industry bodies? Join Mia Spiegelman, VP of Regulatory Affairs at Medtech Canada, for a practical and interactive session designed to demystify the first steps in regulatory and quality careers, highlight the importance of industry feedback to government, and showcase the resources and advocacy work of Medtech Canada.
This session will:
Introduce the regulatory and quality landscape for medical devices in Canada, including essential skills, career pathways, and common challenges faced by newcomers.
Explain the mechanisms and impact of providing feedback to government, drawing on real examples from Medtech Canada’s consultations with Health Canada on regulatory amendments and product shortages.
Showcase Medtech Canada’s role as a bridge between industry and regulators, offering tools, committees, and collaborative platforms to support members in regulatory, quality, and environmental affairs.
This session will provide actionable insights and a roadmap for success in Canada’s dynamic medtech sector.