CELLIANT meets updated requirements for Class 1 Medical Devices in EU

September 28th, 2023

The European Union (EU) has upgraded the requirements for the Class 1 Medical Device designation and Hologenix®, creators of CELLIANT®, has met the stricter requirements for this important market. This means that compliant manufacturers can continue to use the CE mark on their EU products containing CELLIANT. Hologenix has been a trailblazer in achieving regulatory […]

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