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About us


BIOREF was founded in year 1983 in Homburg / Saar (Germany). 1985 BIOREF moved to the present company location (Mömbris, Germany) 50 km east from Frankfurt International Airport. Since this time BIOREF organizes regular proficiency studies. 1987 BIOREF launched it's first tumour marker reference material, which has been improved continuously since then.

Since 1997 BIOREF also produces control sera for hormones and drugs. The product range was expanded several times - now also control sera for cardiac markers, thyroid hormones and plasma proteins can be offered.

BIOREF has established a quality management system since many years which is certified according to ISO 9001 and ISO 13485. This quality management system is continuously adjusted to business as well as official requirements and it is regularly improved for the benefit of our customers. The external surveillance of the quality management system is performed by MDC Medical Device Certification GmbH (Stuttgart, Germany), which is specialized on the certification of medical devices and in-vitro-diagnostic products. The aim of BIOREF's quality policy is to supply the customers with high quality products in order to contribute to the maintenance and improvement of the customers' quality systems.

BIOREF manufactures it's control sera in it's own production laboratory by applying a special production procedure. Therefore BIOREF is also able to produce tailor-made control sera. Analyte content, concentration, filling and packaging can be adjusted according to the customers' needs.  

Please contact us if you wish to receive any further information.

Telephone: +49 (0) 6029 / 5121
E-Mail:
bioref@t-online.de

 


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