FREE Webinar for CAPRA MembersTips and Tricks for the new REP/CESG
Lean about some of the tips and tricks for a successful submission of a medical device licence application or amendment submission using the new Regulatory Enrollment Process (REP) and Common Electronic Submission Gateway (CESG).
GUEST SPEAKER
Shirley Furesz
Director Regulatory Affairs, Medical Devices, Innomar Strategies Inc.
Shirley Furesz
ABOUT OUR SPEAKER
Shirley Furesz is the Director, Regulatory Affairs Medical Devices at Innomar Strategies Inc. She has been working as a regulatory affairs consultant since 2006 and has extensive experience with medical devices, in vitro diagnostics, companion diagnostics and combination products including those used in orthopedics, cardiology, gastroenterology, general surgery, dermatology, gynecology, imaging, respiratory, ENT, urology, wound care, dentistry, infection control, and oncology. Shirley received her Ph.D. in the area of vaccine development from the Department of Veterinary Immunology and Microbiology at the University of Guelph. She provides regulatory strategy and manages a wide range of device submissions for Health Canada and other regulatory agencies. Shirley achieved her Regulatory Affairs Certification (RAC) from the Regulatory Affairs Professionals Society in 2009. Prior to joining Innomar Strategies, she was a key member of the medical devices consulting team at Icon plc (previously Mapi Life Sciences, OptumInsight and CanReg Inc.) and has held various research positions at Syn-X Pharma and NoAb BioDiscoveries Inc. in the areas of Point of Care Diagnostic Kit development, Proteomics, Cell Biology, and ADME-Tox testing.
Registration Closes
Friday, July 17, 2026 at 5 p.m. ET
Friday, July 17, 2026 at 5 p.m. ET
Member Rate -Free | Student Member Rate - Free
Non Member Rate - $80.00 | Non Member (Student) Rate - $25.00
(HST will be added at time of checkout)
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