About Ardena

Trusted, reliable, expert. A CDMO partner that delivers

Ardena is a contract partner delivering pre-clinical and clinical drug development, manufacturing and bio-analysis services to clients internationally.

Quite simply, we’re a CDMO that guides companies through the drug discovery and development process to help create effective and compliant drug products for clinical trials.

Headquartered in Ghent, we have facilities in the Netherlands and Belgium, serving a global customer base, ranging from emerging biotech to tier-one pharmaceutical companies.

Navigating you through drug development.

At Ardena, we understand the challenges of drug development better than most. For many companies, there are limited opportunities to get a promising molecule through clinical trials.

You need your clinical GMP materials and bioanalytical results on time in order to generate your valuable clinical data and reach your next milestone. Naturally, you may face formulation or bioanalytical challenges on your journey that require specialist expertise. You may even lack the in-house capacity to deliver your project. Limited knowledge of regulatory compliance and quality parameters may also be placing your project at risk.

It is for all these reasons that Ardena exists. That’s why we are a trusted, reliable and expert partner for many clients. And why we can navigate you through your drug development journey.