The Quality - A key element of our company

In the EUROBIO, the Quality Services and Regulatory Affairs team consists of six (06) members, ensuring full compliance with regulatory requirements on its products and customers satisfaction.     

  •  A Certified Company

In order to present a well developed and robust quality system, EUROBIO set a Quality Assurance Handbook that describes the quality management system and presents its Quality Policy in relation to the standards requirements:

NF ISO 9001 (v. 2008)–which specifies the requirements Quality Management System requirements - renewed in 2013 in order to demonstrate our ability to consistently supply a product that meets our customer’s requirements and increase their satisfaction.

NF ISO 13485 (v.2012)– which specifies Quality Management System requirements for Medical Devices Industry -Requirements for regulatory purposes renewed in 2013 demonstrating our commitment to achieve a quality service, to comply with regulations and to meet our customer’s expectations.

The Quality Policy established by EUROBIO is to develop, implement and continuously improve the Quality Management System. It aims to improve customer’s satisfaction, reduce the number of disruptions and delays in deliveries, and develop the tools necessary for our products international development ... all this in order to meet our client’s requirements.




  • A Committed Company

Striving for continuous improvement, we are committed to a sustainable environmental policy since 2011 with the opening of an environmental policy aimed to improve, prevent and control our impact on the environment.

The company also has a Sustainable Development policy.

These environmental efforts of EUROBIO gradually lead the way to finally obtaine the ISO 14001V2004 certification on October 1, 2014.

We operate on a geographic scale of our activities to reduce the environmental impact of our projects and activities.

We are committed to reduce our energy, paper and water consumption and properly manage our wastes.

  • Quality Products

The CE trade mark on our products demonstrates our commitment to comply with the normative and regulatory framework related to our different products to satisfy more customers and to guarantee the our product’s quality.

We especially comply for some of our products the Directive 93/42 / EC Medical Devices and the Directive 98/79 / EC Diagnostic Medical Devices in Vitro.

It is also important to note that EUROBIO manufactures and markets product therapeutic annex for which we have received marketing authorization from our French competent authority, the ANSM.


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