Digital Edition: Market Pathways February 2025

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ARTICLE SUMMARY:

A panel of medtech leaders opines on the current state of coding, coverage, and payment; Trump’s FDA retreats from the standards development process; a side-by-side comparison of device supply chain reporting rules in the US and EU; CMS' draft guidance on real-world evidence study protocols; and in Consultants’ Corner, expert tips on the new EU pathway for orphan devices.

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