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Mantra Systems provides a full suite of MDR & IVDR consulting services to companies worldwide seeking access to EU & UK markets for any class of medical device.
Our medically-trained consultants & subject matter experts will bring specialised clinical evidence appraisal & analysis to your medical device regulation strategy.
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Resources for Medical Device Regulation
Our Medical Device Regulation Resources contain information and guidance on a wide range of subjects across the regulatory landscape.
For further guidance or any specific enquiries, please contact our specialist consultants.
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EU MDR Compliance Guide
A free Medical Device Regulation guide
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