CE Labelling and Quality Management

MRC supports your products in all steps of the development life cycle. We can also guide you through the processes required for CE labelling of medical products, like risk management, application of harmonized standard, documentation of general requirements.

MRC has established a Quality Management System in accordance with the ISO 9001, ISO 46001, and MDD in 1998. We have updated our processes to the new requirements of EN ISO 13485, the standard for medical products. Our work processes integrate the high demands of medical product development & manufacturing with the force of analytical and creative engineers.

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