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.
Medical Device Industry Executives
Regulatory Affairs Professionals and Management
Quality Professionals and Management
Clinical Affairs Professionals and Management
R&D Engineers and Management
Greenlight Guru is a modern quality management software platform used by medical device companies in over 600 cities and 35 countries to bring new products to market faster while simplifying regulatory compliance and reducing risk. Being the only industry specific, cloud-based eQMS,
Greenlight Guru is easier to implement, easier to use and simply fits medical device processes out-of-the-box allowing companies to innovate faster and be more efficient. Visit our home page to learn more.
Rook Quality Systems provides specialized and custom consulting services for all classes of medical devices. We work with you to outline your quality and business goals to develop innovative and efficient practices that improve compliance and profit. To see a full list of the services Rook offers you can go here.