In iDNA Laboratories, with quality and scientific reliability as our main pillars, we have adopted a Quality Management System that allows the control of all the company's processes.
In this context, the company is certified according to the international standards ISO 13485:2016, ISO 27001:2013 and ISO 9001:2015 for the research, design, development, production and sale of in vitro diagnostic medical devices related to pharmacogenomics and genetic analysis.
It also applies the Principles and Guidelines for Good Distribution Practice for Medical Devices in accordance with the Ministerial Decision ΔΥ8δ Γ.Π. οικ 1348 2004.
ISO 13485: 2016 for the promotion, sale and distribution of in vitro diagnostic medical devices related to the Pharmacogenomic analysis
ISO 9001:2015
for Quality Management
ΙSO 27001:2013 for Information Management
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