Medevise Consulting brings together an experienced team to provide regulatory, clinical, market assessment and medical communication services for ophthalmic companies looking to succeed in Europe.
With unparalleled insight, resources and a network built up over decades of experience, we work with clients to build long-term relationships that ensure your European business thrives. As a team of specialists, we stand for ophthalmology innovation in Europe.
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Click below to schedule a 30-minute complimentary consultation with our senior team. We look forward to discussing your business and how Medevise can support you in reaching your clinical, regulatory, market access, and communication goals.
MDR + CE Mark Topics
Listen as we break down the recent changes to the MDR and the impact for manufacturers, with legal expert Erik Vollebregt of Axon Lawyers.
We discuss the difficulties companies face with MDR, how it emphasizes clinical evaluation & strategies for the Blue Guide incongruency.
This article highlights key issues from RMD, including how the new MDR impacts medtech with AI or software & the state of notified bodies.
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