Medical Devices
Date: March 22, 2010
Location: Marriott Eaton Centre Hotel
525 Bay Street, Toronto
More information:
Visit www.oha.com/conferences for program updates and information.
A number of new developments set the stage for this year’s conference in Toronto. Find out – from experts in all areas of the medical devices sphere – what these developments mean to you and your organization:
Get up-to-date on Health Canada requirements, and the industry Code of Conduct for interactions with health care professionals.
From Stephen Dibert – President & CEO of MEDEC
Receive clarity on the recent classification of patient management software as a medical device – the unclear effects of which have caused confusion among health care organizations.
From Sarah Chandler – A/Head, Regulatory and Scientific Section Device Licensing Services Division, Medical Devices Bureau, Health Canada
Hear practical tips from case studies on managing risk and liability exposure in reprocessing.
From Mitra Nadjmi – Senior Risk Management Specialist at the Healthcare Insurance Reciprocal of Canada, and Tim Buckley, Partner at Borden Ladner Gervais LLP
Become current on the key issues surrounding the reprocessing of single-use implantable components that are part of surgical instrument sets.
From our Feature Speaker, Dr. Michelle Alfa – Medical Director, Microbiology Discipline Diagnostic Services of Manitoba, St. Boniface General Hospital
And more.