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Online Webinar
01 Mar 2011

Introduction to ISO 13485 Quality Management

This is an introductory course for section by section understanding of ISO 13485 requirements of a quality management system.

Why You Should Attend:All EU member states and satellite countries, Canada, Japan and Australia, require registration to ISO 13485 to sell your medical devices. Development and implementation of a quality system that is compliant with ISO 13485 requires many resources and personnel. ISO 13485 is a wordy standard, drafted by individuals for many of whom English is not their primary language! This webinar provides a section-by-section review of ISO 13485 in a clear concise manner, and provides suggestions for development of a compliant system.Areas Covered in the Seminar:What is ISO 13485, and what does a company need to do to Register to ISO 13485?Purpose and structure of ISO 13485.Systemic Requirements.Management Requirements.Resource Requirements.Realization Requirements.Remedial Requirements.Implementation of an ISO 13485-compliant quality system. 


1 Mar 2011 @ 10:00 am

1 Mar 2011 @ 11:00 am

Duration: 1 hours



Online Webinar


English en

Organised by

ComplianceOnline (deactivated)

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