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.
Who Will Benefit:
This webinar will provide valuable assistance to all device manufacturers who wish to have a better understanding of the requirements of ISO 13485. The employees who will benefit include:
- Top management
- Regulatory management
- Quality Management
- Documentation Management
- Quality Engineers
For More Information:
Note: Use this promocode(117660) for 10% discount.