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Medical Device Regulatory Compliance Experts

MedQtech AB is a consultant company in the medical device industry. Experienced professionals with high competence who support customers in the fields of Quality and Regulatory compliance. We have broad experience in Medical Device Industry, MDR, IVDR, ISO 13485, ISO 14971, IEC 62366-1, IEC 62304, QSR (FDA 21 CFR Part 820, Part 11) and other regulations and standards in medical device industry.