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    Achieving and Maintaining Regulatory Compliance is our speciality.

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Following the requirements of the MDR and the guidance of the MEDDEV 2.7/1 revision 4

Confirmation of conformity with relevant general safety and performance requirements of Annex I of the MDR, goes through planning, conducting and documenting a clinical evaluation in accordance with the MDR requirements. The research and scientific background of our team allows us to perform this work, with the input of your device experts.

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