As an EN ISO 13485:2003 + AC 2007 and EN ISO 9001:2008 certified company all STRATEC Molecular products are subject to extensive quality control. In compliance with Directive 98/79/EC on in vitro diagnostic medical devices (IVD-Directive)* many STRATEC Molecular products are CE-marked. STRATEC Molecular guarantees the correct function of all products and highest quality support by first-class service.
*) Products which are CE-marked according to the IVD-Directive can be used for diagnostic applications in countries where this directive is recognized.