Susan Dew

Susan Dew is the Associate Director of Regulatory Affairs at Abbott Point of Care, where they lead the team responsible for international regulatory compliance and submissions for products. Previously, they held various roles including Director of QA Operations at Abbott Point of Care, QA Director at Nordion, Quality Control Manager at MDS Nordion, and Regulatory Affairs Associate at Canadian Blood Services. Susan's educational background includes ongoing studies towards a Quality Assurance Management Diploma at the University of Manitoba, a BSc in Chemistry and Microbiology from the University of Alberta, and coursework in a Master's in Management from the University of Ottawa. Their extensive experience spans both regulatory and quality assurance functions in the healthcare and pharmaceutical sectors.