Morningside posted a video "Meeting MDR & IVDR Regulations_ Translation & Cost Saving.mp4" on VIMEO

Keeping up with the evolving MDR and IVDR regulations can challenge medical device manufacturers. Although the EU Commission has adopted a proposal to give more time to medical device manufacturers, now is the best time to ensure you have a strong understanding of the new and changed translation regulations for both MDR and IVDR set to be implemented progressively between by 2025 and 2028.To ensure there is no shortage of your life-saving medical products in the EU, join MDR and IVDR expert Carlos Galamba, Co-Founder of MDx CRO and Vice President of IVD Intelligence and Innovation at RQM+ and Anna Eisenberg, Associate Director of Life Science Business Development of Morningside, a Questel Company where they will cover:How to Get MDR & IVDR CertifiedWhat to Expect With New & Changed Regulations for MDR & IVDRHow to Meet Translation Requirements for MDR & IVDRTranslation Best PracticesTranslation Cost-Saving Tools