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For Manufacturers The CMDR & ISO 13485:2003 Meeting the Canadian requirements Very good explanation of the structure of the Canadian Medical Devices Regulations (CMDR), along with the relationship to CMDCAS. This will allow my company to integrate the CMDR into the quality system. Deb Harney Zimmer inc.   ABBREVIATIONS MTL Montreal QUE Quebec CHI Chicoutimi OTW Ottawa ASI Asia TOR Toronto ATL Atlantic Provinces EU Europe USA United States WEB Cybercourse   CYBERCOURSES - All times shown are Montreal, Canada times 2011     COURSES JAN FEB MAR APR MAY JUN Introduction and overview of the Canadian Medical Devices Regulations For manufacturers, importers and distributors of Medical Devices sold in Canada                   Awareness and information 2011     COURSES JAN FEB MAR APR MAY JUN A role play on quality Quality management awareness for employees   In-house sessions only   ISO 9001:2000 Top management awareness   In-house sessions only     Auditing the management system 2011     COURSES JAN FEB MAR APR MAY JUN Internal auditors On-the-job internal auditing of processes Adding value with the PDCA approach   In-house sessions only     Medical devices 2011     COURSES JAN FEB MAR APR MAY JUN CMDCAS - Training     14 - 15 OTW       02 - 03 OTW   Presented in Frankfurt, Germany - this course is now full CMDCAS - Training Using ISO 13485:2003                   Laboratories in medical biology 2011     COURSES JAN FEB MAR APR MAY JUN Biomedical Laboratories ISO 15189 Understanding one’s role in the quality management system   In-house sessions only     Laboratories 2011     COURSES JAN FEB MAR APR MAY JUN ISO/IEC 17025:2005 Internal auditing course For laboratories   In-house sessions only   For a successful implementation ISO 15189:2007   In-house sessions only   Overview of ISO/IEC 17025:2005 For scientific and technical personnel (forensic labs)   In-house sessions only   Overview of ISO/IEC 17025:2005 For scientific and technical personnel   In-house sessions only   ISO/IEC 17025:2005 Technical assessor course   In-house sessions only     Automotive industry 2011     COURSES JAN FEB MAR APR MAY JUN Advanced Product Quality Planning [APQP]   In-house sessions only   Overview of the Core tools - Automotive Industry APQP, FMEA, SPC, MSA, PPAP   In-house sessions only   Failure Mode and Effects Analysis [FMEA]   In-house sessions only   ISO/TS 16949:2009 For a successful implementation   In-house sessions only   Production Part Approval Process [PPAP]   In-house sessions only     Tools for continuous improvement 2011     COURSES JAN FEB MAR APR MAY JUN Process Approach Improvement of work processes   In-house sessions only   Process approach Mapping and documenting processes Management system   In-house sessions only   Process Approach Statiscal control of work processes   In-house sessions only     Specialties 2011     COURSES JAN FEB MAR APR MAY JUN Introduction to Sterilization processes Medical devices   In-house sessions only   Top

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