Mediteq Forum Meating – Digitalt – How to make the Canada goose fly?
Mediteq Forum is excited to welcome Mia Spiegelman from MedTech Canada as guest speaker
to this webinar focusing on the regulatory requirements and medical device landscape in Canada.
In this session, Mia will share what the regulatory requirements look like for the Canadian market and how the registration process is structured. She will also talk about MDSAP and what that means for a manufacturer entering the Canadian market. She will share her insights and information on recent changes and possible impacts, as well as her best advice and no-go to be successful on the Canadian market.
Mia Spiegelman is Vice President, Regulatory, Quality and Environmental Affairs at Medtech Canada. She holds a B.Sc. in Chemistry from York University and a Certification in Pharmaceutical Regulatory Affairs and Quality Operations from Seneca College.
With 26 years of experience across the medical device, pharmaceutical, cosmetic and consulting sectors, Mia has held diverse Quality and Regulatory Affairs roles. At Medtech Canada, she leads strategic regulatory, quality and environmental initiatives that support members and a globally competitive Canadian regulatory environment. She was recently elected Co-chair of CSA Z289 and the ISO/IEC mirror committee (TC 210) and joined CUBEC’s Strategic Board of Advisors.
Place: Digitalt Zoom meating
Date: 24th of November, from 15.00 – 17.00
Program: Länk
Sign up: Länk