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Webinar 9: How to set up post-market surveillance

A review of ISO 14971 requirements and practical tips to set up an efficient and effective post-market safety surveillance process for your medical devices.

💥Medical device manufacturers are required to establish an effective post-market surveillance process as part of their quality system to ensure continued safety and effectiveness of their products.

👉This proves to be very difficult in practice. One reason is that a lot of resources are taken up by the Complaints Handling process required for regulatory…

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