Preparing for ISO 13485:2016
ISO 13485: 2016 is the quality management backbone for many medical device manufacturers. This standard has recently been revised, with significant updates to the requirements. The new version was published in March 2016 and companies must complete their transition by March 31, 2019. Do you know what the updates are and what you need to do to stay in compliance?
It is time to plan. Attend this educational webinar to learn about the changes that have been made and best practices to help you transition to ISO 13485: 2016 compliance.
This Webinar Will Highlight:
- Regulatory Requirements: a brief overview of why we are where we are
- Significant changes introduced in ISO 13485:2016
- Using a Product Lifecycle Management (PLM) system to integrate risk and applicable regulatory requirements
Educational Webinar: Preparing for ISO 13485:2016
Thursday the 6th of September 2016
7:00 PM (CEST)