MDD to MDR Transition Timeline

A Quick Snapshot on #MDR / #IVDR Transition
While the European Commission and the European Union have finally approved the #TransitionalTimelines for certain medical devices, as a Manufacturer, it is now your duty to ensure complete compliance with the Regulations.
What should a Medical Device Manufacturer do with the EU MDR Transitional Deadlines?
🔨 Make sure your #QualityManagementSystems are in Place.
🔨 Ensure appropriate Transition plan from EU Medical Device Directives [EU MDD] to EU Medical Device Regulation are in Place.
🔨 Contact Experts at Med-Di-Dia who can support you with completing your transition plans, technical files and documents.
🔨 If you are yet to launch your medical device on the EU Market, speak to our experts, who can create the right Regulatory Roadmap for a smooth launch.
We are here to be your Regulatory Risk Partners for Medical Devices, Diagnostics and Digital Health!
Drop us an email at [e-mail]
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#YouInnovate we shall partner your #RegulatoryCompliance
#MedDiDia #PRRC #EUAR #USFDA #MDR #IVDR #MedicalDevices #Diagnostics #DigitalHealth #QMS
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