Validation Support for Satisfying the New Medical Device Regulation


Invotec is now offering a new equipment validation program to support medical device manufacturers facing implications from the new European Medical Device Regulation (EU-MDR).   Set to take effect this year, the EU-MDR will require medical device manufacturers to meet higher documentation requirements within a shorter reporting deadline—meaning many manufacturers are facing a significant increase in effort during the validation process.   Invotec is here to help. Over the past six months, we have been working to develop a standard … Read More