I hold a bachelor in biochemistry from McGill University and a master degree in immunology and virology from the INRS – Institut Armand-Frappier.

I started my career doing preclinical research in a biotechnology company. This first experience is a tremendous asset when it is time to understand the various scientific concepts behind the development of innovative drugs and medical devices.

Then, I was a major player in the setup of the CRO-Operation division of a now well-renowned clinical research organization.

Throughout the years, I acquired an extensive knowledge of all aspects of clinical research with specialization in Canadian regulatory affairs and medical writing.

I have experience with pharmaceutical drugs, biological drugs, natural health products, cosmetics, and medical devices.

In 2017, I deepened my knowledge of the Canadian regulations by earning the RAC (Regulatory Affairs Certification) credential.

Since then, as a freelancer, I share my knowledge with companies and investigators who need assistance to reach their objectives.

I’m available as a temporary resource to overcome occasional increases in the workload, to assist with a new task, or for a long-term collaboration.

• Regulatory Affairs Certification (RAC) – Canada by the Regulatory Affairs Professionals Society (RAPS)

• Canadian Association of Professionals in Regulatory Affairs (CAPRA)
• Regulatory Affairs Professionals Society (RAPS)
• American Medical Writers Association (AMWA)