The time it takes for a medical device can hit the market can be critical in a competitive landscape. As technologies continue to evolve, manufacturers need to understand different medical device markets and what it takes to gain approval and be compliant in different geographies. This guide include infomation on medical device markets, emerging trends, current regulations, market adoption strategies, and vendor selection.
One major shift in recent years has been the differences in the pathway to approval between MDR and the FDA. We cover these changes, harmonized differences, and considerations manufacturers will want to make when choosing a compliant power supply that can make the approval process faster, no matter where they are planning to sell their devices.
If you have additional questions or insights you’d like to see addressed or included in this guide, please contact us. You can download a PDF copy by filling out the form.
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