Ordina assists companies in the pharmaceutical and biotechnological sector with the optimisation of production processes, automation of systems, software implementation and computer system validation. Safety and efficiency are crucial in your sector. Research, development, production and distribution are therefore subject to strict rules, both global and local. Examples are the cGxP guidelines of the Food & Drug Administration (FDA) and the European Medicines Agency (EMA). In every step of our cooperation we proceed in a very controlled way, in accordance with all national and international regulations. The whole process is carefully documented. So you can be sure of qualitative processes that pass every audit with flying colours. Q, Ordina’s Quality and Compliance team, is the quality partner of pharmaceutical and biotechnology companies. 70 experts from different backgrounds, such as industrial engineers, bio engineers, biomedicals and pharmaceutical experts, are at your service. But also historians, translators/interpreters, communication scientists, etc. regularly find their way to our team. They help you to validate and qualify your material, processes and software. Can you use help to optimize your production processes, automate systems, implement software or validate laboratory systems in this highly regulated market? Our team knows how to hit the whip.