Vali­da­ti­on Sup­port for Satis­fy­ing the New Medi­cal Device Regu­la­ti­on

InvotecNews

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