How to Ensure Compliance with the New EU Medical Device Regulations: MDR & IVDR
September 17, 2018 - Toronto ON CA

Xtalks

fbonilla@xtalks.com
Phone: 4169776555

Register for this webinar to learn: The key changes that are occurring under the new regulations How to prioritize your product portfolio The importance of early planning in preparing clinical studies to certify new devices and to recertify existing ones How early transition can give your products an advantage in the market

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