Having an effective PMS system is important from both a regulatory and quality perspective.
This webinar will help manufacturers to learn about the key requirements, concepts and the overall process for post-market surveillance under the MDR.
Based on regulatory requirements and operational tools provided during the webinar, you will be able to write your PMS documentation that includes both proactive and reactive sources of information.
Fill in the form to request your webinar recording.
Please be sure not to use accented letters as they are not recognised by the system.