FREE ON-DEMAND WEBINAR
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.