ISO 13485 for Medical Device QMS

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This webinar will provide valuable assistance to all device manufacturers who wish to have a better understanding of the requirements of ISO 13485.

Development, implementation, and maintenance of an ISO 13485-compliant quality management system requires many resources and personnel to meet with success. ISO 13485 is a wordy standard, drafted by individuals for many of whom English is not their primary language. This webinar is 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 Session:
The purpose of the standard
Standard structure
Section-by-section requirements
Section-by-section Implementation approach
Who Will Benefit: The employees who will benefit include:
Top management
Regulatory Management
Quality Management
Documentation Managers
Quality Engineers
Other personnel involved in development and implementation of the QMS