Medical Devices Shipping for Processing and Trials
Shipping medical devices for processing and trials involves a complex regulatory framework, particularly under the EU’s Medical Device Regulation (MDR) 2017/745 and In Vitro Diagnostic Medical Device Regulation (IVDR) 2017/746. These regulations impose strict requirements on relabeling, repackaging, and translating device information to ensure compliance, which is essential for smooth cross-border medical device shipping.
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