ISO 13485:2016

IQ’s quality system is based on ISO 13485, published in 2016, and dictates quality-management standards and requirements for a comprehensive management system for design and manufacture of medical devices. IQ has met ISO 13485 conditions as well as 21 CFR 820 corresponding subparts. The company is ISO13485:2016 certified by DEKRA Certification B.V. for all activities, including research & development, manufacturing and marketing & sales.


By internal and external audits we actively maintain and improve our quality system. Our current certificate is dated on February 1, 2019 and will be valid until February 1, 2022.

In May 2019 IQ Products was audited with respect to the South Korean KGMP requirements and obtained approval to manufacture in vitro diagnostic devices for the Korean market. We are happy to work together with our distributor Dow Biomedica to facilitate CMV antigenemia testing.


ISO 13485-2016 certificate

CE certificate CMV pp65 detection kits

Declarations of Conformity

CMV Products
Fetal Cell Count
FMH QuikQuant
Monoclonal Antibodies

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Terms and conditions

Our delivery terms and conditions

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IQ Services BV
Rozenburglaan 13a
9727 DL Groningen
The Netherlands

Tel +31 (0) 50 5757000
Fax +31 (0) 50 5757002
E-mail info@iqservicesbv.nl