±«ÓãÖ±²¥
Graduate Program Director
Ìý Ìý ÌýPh.D., ±«ÓãÖ±²¥ (Electrical Engineering)
Ìý Ìý ÌýPost-Doctoral Fellow, Université de Montréal (Montreal Clinical Research Institute)
Ìý Ìý Ìý•ÌýClinical Trials
Ìý Ìý Ìý• Artificial Pancreas
Ìý Ìý Ìý• Electrical Engineering
Ìý Ìý Ìý• Mechanical Engineering
Ìý Ìý Ìý°ä´Ç°ù±ðÌý°ä´Ç³Ü°ù²õ±ð: BMDE 655 Biomedical Clinical Trials - Medical Devices
Ahmad Haidar
Associate Professor, Biomedical Engineering
Industry Expert Faculty
Ìý Ìý ÌýPatent Agent, Canada (CIPO) & United States (USPTO)
Ìý Ìý Ìý• Intellectual Property
Ìý Ìý Ìý• Medical Devices and Software
Ìý Ìý Ìý• Drafting and Prosecution
Ìý Ìý Ìý• B.Eng, Mechanical Engineering, ±«ÓãÖ±²¥
Ìý Ìý Ìý°ä´Ç°ù±ðÌý°ä´Ç³Ü°ù²õ±ð:ÌýBMDE 653 Patents in Biomedical Engineering
Pierre T. Nguyen
Ìý
, Partner, Norton Rose Fulbright
AffiliateÌýMember, Department of Biomedical Engineering
Ìý Ìý ÌýConsultant, Medical Device Quality Management & Regulatory Affairs
Ìý Ìý Ìý• Quality Management Systems (ISO:13485)
Ìý Ìý Ìý• Regulatory Affairs (Health Canada, FDA, CE)
Ìý Ìý Ìý• Consulting
Ìý Ìý Ìý•ÌýB.Eng., Mechanical/Industrial Engineering, Concordia University
Ìý Ìý Ìý°ä´Ç°ù±ðÌý°ä´Ç³Ü°ù²õ±ð:ÌýBMDEÌý654 Biomedical Regulatory Affairs - Medical Devices
Danny Kroo
Ìý, Medical Device Quality Management & Regulatory Affairs (QA/RA)
AffiliateÌýMember, Department of Biomedical Engineering
Ìý
Ìý Ìý ÌýChief Technology Officer (CTO)
Ìý Ìý Ìý• Medical device design & development
Ìý Ìý Ìý• Design inputs & outputs, risk management, documentation
Ìý Ìý Ìý• High-risk medical devices / regulatory approvals
Ìý Ìý Ìý• B.Eng., Mechanical Engineering, Toronto Metropolitan University (fka Ryerson)
Ìý Ìý ÌýCore Course: BMDE 656 Medical Device Development Process
André Tremblay
Ìý, Agile MV
Ìý