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ISO 13485 for Medical Device QMS

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

Who should attend?

Top management Regulatory Management Quality Management Documentation Managers Quality Engineers Other personnel involved in development and implementation of the QMS

Details

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

Prices

Price List: Live : $245.00 Corporate live : $995.00 Recorded : $295.00

Contact

david ross
davidross759@gmail.com

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