HOW TO CONQUER SUPPLIER MANAGEMENT FOR MEDICAL DEVICE COMPANIES

As a device manufacturer, it is your responsibility to ensure the components and suppliers used in the manufacturing of your device meet your defined requirements. 

This process of purchasing and supplier control is becoming more detailed in the ISO 13485/ 21 CFR 820/ MDSAP/ MDR regulations and can lead to unfortunate surprises during your audit if you have not updated your processes accordingly.

This webinar outlines the details within the standards, how to update your procedures, and best practices on documenting your supplier approval and evaluation.

SPECIFICALLY This Webinar will Cover:

• Overview of purchasing and supplier control in ISO 13485, 21 CFR 820, and upcoming changes to meet MDSAP and MDR requirements
• How to create an effective supplier evaluation process
• Incorporating risk into supplier evaluation and review
• Best Practices for efficient supplier management
• How Quality effects Supplier Agreements

Who should attend?

• Medical Device Industry Executives

• Regulatory Affairs Professionals and Management

• Quality Professionals and Management

• Clinical Affairs Professionals and Management 

• R&D Engineers and Management