CASE STUDY

A global medical device manufacturer reduced release authorization workload by 88%

Read our free case study to discover how Rimsys digitized and automated global medical device registrations for a $2 billion neuroendovascular technology company with 15,000 products in 100+ countries, utilizing an off-the-shelf, product-centric global medtech regulatory software platform.

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A global medical device manufacturer reduced release authorization workload by 88%

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Quick reference guide - global medical device UDI requirements and timelines
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