Immundiagnostik has been developing and producing laboratory diagnostics at the highest level since 1986.
As a manufacturer of in-vitro diagnostics, we subject the Medical Devices Act and Directive 98/79 / EC on in-vitro diagnostics. Our quality management system is certified according to DIN EN ISO 13485. The majority of our products are marketed with a CE mark after they have been tested in clinical and scientific practice as part of collaborations within our intensive academic network.
In addition to the constant quality control in our company, we regularly and successfully take part in voluntary external quality controls, such as the proficiency testing of INSTAND e.V. Our customers, have always had great success with our products when they participate in these independent quality controls, too.
This quality creates trust and has formed the basis of our company's success for over 30 years.
If you would like to receive the complete certificates, please contact us at: International Sales