CSA Medical Device Workshop
Attend this Workshop and learn the what, who, and how for a
smooth certification process
CAN/CSA 222.2 No 60601-:08 (IEC 60601-1:2005 3rd Edition and its impact on the certification process for Test Houses and Manufacturers
October 29, 2009, 9:00 am to 4:00 pm
Toronto, Ontario
REGISTER NOW!
Facilitator: Hans-Werner Zeller, Engineering Manager, Electronic Products, Europe
Description
This timely and informative Workshop will give attendees an indepth look into the most important changes of requirement of the Standard and its impact on the design and certification process. It will demonstrate the steps and processes of how and what a Test House will require to certify a M.E.E. (Medical Electrical Equipment) according to the new Standard.
The facilitator will provide practice oriented examples and a hands-on exercise on the process for obtaining a successful certification.
Objective
Attend this timely workshop and:
- gain an understanding on what to expect from a Test House for a successful certification process
- get a detailed explanation of all North American deviations
- understand how a Certification Body will certify a Medical Device under the new process oriented requirements
- learn how to interpret and implement the new approach and requirements
WHO SHOULD ATTEND
Regulatory Affairs Managers/Professionals, Safety and Regulatory Compliance Engineers, Compliance Managers & Design Engineers.
WORKSHOP FEE: $695 CAD
Get an additional 10% off your Symposium Registration!
Register for both the Symposium and this seminar!
Registration Fee includes a Complimentary copy of PLUS 14971:2007 and IEC TR62348
