The firm provides advice and support in relation to the regime of health records and sanitary surveillance of in vitro diagnostic reagents for examinations of specimens of human origin regulated by Decree 3770 of 2004 and in vitro diagnostic reagents orphan, in vitro analytical grade, specific analyte, reagents for general use in laboratories and in vitro reagents in research used in samples of human origin regulated by Decree 1036 of 2018.

Similarly, Resolution 000132 of 2005, which requires all importers to comply with a specific quality system for the storage of their products, our auditors offer in this case the possibility of preparing for the visit and later obtaining the Certificate of Conditions of Storage and Conditioning, necessary to obtain the Sanitary Registry.