RQ_Webinar_April_2018_Promo-min

The requirements and staff it takes.

The EU MDR lays out requirements for a proactive post-market surveillance system that that inputs into the ongoing risk management and clinical evaluation processes throughout the device life cycle. In this webinar, we’ll cover the requirements for the PMS system, PMS planning, and PMS reporting. With significant new requirements for device-specific plans and reports, you’ll need to update your post-market surveillance system with enough time for your staff to implement the changes.

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