Quality is key in everything we do. As a partner, you are relying on that. Our entire organisation works according to a quality management system that meets the requirements of the NEN-EN-ISO 9001:2015 standard. The Quality Assurance team monitors the application of the quality standards and plans internal audits and feedback sessions.

Our state-of-the-art laboratory has been NEN-EN-ISO/IEC 17025:2017 accredited by the Dutch Accreditation Council (RvA) for a large number of laboratory tests (registration number L120 Testing).

We conduct evaluations and studies in accordance with international standards and guidelines such as the European Pharmacopoeia (Ph. Eur.), VICH and WOAH. We can conduct studies in compliance with the OECD principles of Good Laboratory Practice (GLP) and have obtained an endorsement of compliance from the Dutch GLP inspectorate.

If required, we have the expertise, infrastructure, and rigorous processes in place to conduct studies in full compliance with Good Clinical Practices (GCP). Our meticulous approach guarantees the integrity, reliability, and traceability of your study data. 

In addition, we maintain an information management system that meets NEN ISO/IEC 27001:2022 requirements. Big data is becoming increasingly important in our field of expertise and can therefore no longer be viewed separately from information security.