An Exclusive Look at the New Changes to ISO 14971:2019 and ISO TR 24971:2019

This on-demand webinar hosted by Greenlight Guru focuses on the new changes to ISO 14971:2019 and ISO TR 24971:2019, providing insights into the latest revisions of these important standards in medical device risk management. Main points covered: 1. Detailed examination of the updates to ISO 14971:2019 and ISO TR 24971:2019. 2. Reasons behind these changes. 3. Preparations for the upcoming changes in the standard. 4. Information about the reorganization of informative annexes. 5. Clarifications on the EU's perspective and the future of harmonized risk management standards. Target Audience: • Medical Device Industry Executives • Quality Professionals and Management • Regulatory Professionals and Management • Clinical Affairs Professionals and Management • R&D Engineers and Management Access the printable slides for this presentation here: https://www.greenlight.guru/webinar/iso-14971-2019-iso-tr-24971-new-changes