Auto­ma­ti­on for Medi­cal Device Manu­fac­tu­rers in Min­ne­so­ta

InvotecNews

While many auto­ma­ti­on and equip­ment pro­vi­ders ser­vice custo­mers from a wide varie­ty of indus­tries, Invo­tec is proud to focus on sca­ling assem­bly, test, and inspec­tion solu­ti­ons exclu­si­ve­ly for medi­cal device manu­fac­tu­rers. In the arti­cle below, Manu­fac­tu­ring in Focus talks with our experts to learn more about what that means for custo­mers in this uni­que industry—specifically tho­se clo­sest to our new faci­li­ty in Min­nea­po­lis, MN. *This arti­cle was ori­gi­nal­ly published in Manu­fac­tu­ring in Focus (July 2020). You can view the ori­gi­nal … Read More

Invo­tec’s Respon­se to COVID-19

InvotecNews

A Mes­sa­ge to Our Custo­mers and Our Com­mu­ni­ty During the COVID-19 Pan­de­mic Dear Valued Custo­mer: As we con­ti­nue to pro­cess the unpre­ce­den­ted emer­gen­cy cau­sed by the COVID-19 pan­de­mic, we wan­ted to reach out to you with an update on how Invo­tec is approa­ching the situa­ti­on. Our prio­ri­ty lies in pro­tec­ting the health and well-being of our employees, custo­mers, ven­dors, and com­mu­nities. Tog­e­ther we con­ti­nue to moni­tor the situa­ti­on daily—developing poli­ci­es and pro­ce­du­res as new infor­ma­ti­on beco­mes avail­ab­le. Employees who are … Read More

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

Join Us at Phar­ma­pack Euro­pe 2020

InvotecNews

  Invo­tec GmbH offers equip­ment vali­da­ti­on as part of com­pa­nies’ pro­cess vali­da­ti­on Vil­­lin­gen-Schwen­­nin­­gen, Ger­ma­ny – The new Invo­tec pro­cess offers sup­port for com­pa­nies to satis­fy the new European Medi­cal Device Regu­la­ti­on (EU-MDR). 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 … Read More

Invo­tec Joins Day­ton Regio­nal Green as a Cer­ti­fied Green Busi­ness

Sarah SpeltzNews

Equip­ment manu­fac­tu­rers are not his­to­ri­cal­ly known for their efforts to go green. But at Invo­tec, we chal­len­ge our­sel­ves to make small chan­ges that add to the sustai­na­bi­li­ty of our envi­ron­ment. Tha­t’s why we recent­ly joi­ned Day­ton Regio­nal Green as a Cer­ti­fied Green Busi­ness. Some of our con­scious busi­ness ope­ra­ti­ons inclu­de using LED ligh­t­ing throughout our US faci­li­ties and solar panels at our Ger­ma­ny loca­ti­on. Addi­tio­nal­ly, all loca­ti­ons use elec­tric for­klifts and recy­cle mate­ri­als whenever pos­si­ble. But most import­ant­ly, our pre­ven­ta­ti­ve … Read More

[FREE PASS] Join Us at MD&M Min­nea­po­lis

Sarah SpeltzNews

Join us as the lar­gest med­tech show in the Mid­west cele­bra­tes 25 years of inno­va­ti­on. Invo­tec will be at the show high­ligh­t­ing the latest capa­bi­li­ties in assem­bly, test, and inspec­tion equip­ment. Click the ban­ner to get your FREE expo pass and join us at the show!