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All the technical and scientific checks carried out during every stage in the development of molecular diagnosis and pharmacogenetic tests must meet the strictest quality standards.


All products selected and developed by LCM Genect are CE-marked in compliance with EU directives. LCM has applied for ISO 9001 and ISO 13485 certifications.


LCM Genect can count on LCM Group’s long tradition in the pharmaceutical industry and on its know-how in the regulatory, distributive and market fields. LCM SpA was the first Italian trading company authorised by AIFA to import Active Pharmaceutical Ingredients.


For further information please visit lcm-group.it


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