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Maud Richard is currently the Quality Assurance Regulatory Affairs Director at Aifred Health. Maud has over 17 years of experience in the medical device industry, with a focus on quality assurance and regulatory affairs.

Maud started their career as a Biomedical Engineer at CdR HSCM, where they worked for 4 years. Maud then transitioned to Duoject Medical Systems, where they spent 13 years working their way up from Compliance Engineer to Director, Quality Assurance and Regulatory Affairs. In January 2020, they left Duoject to join Aifred Health as their Quality Assurance Regulatory Affairs Director.

Maud Richard has a Masters in Biomedical Engineering from Polytechnique Montréal as well as a Bacc in Electrical Engineering from Université de Sherbrooke. Maud is also certified from RAPS in Regulatory Affairs Certified (RAC), Regulatory Affairs Certification Program in RAPS Member, and Regulatory Affairs Certification Program in RAC-US.