Navigating you through
We are Ardena, a fully integrated Contract Development & Manufacturing Organization (CDMO) with a core focus on bringing molecules to the clinics.
One dedicated and integrated partner for your early phase development journey.
Full service offering covering chemistry & pharmaceutical development, product and bioanalytical support and CMC dossier development services.
More ways we can support you...
Your expert guide through early phase drug development. Your molecule, your milestone, our mission.
We’re a pharmaceutical 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 (Belgium), we also have facilities in the Netherlands, Sweden and Latvia. We serve a global customer base, ranging from emerging biotech to tier-one pharmaceutical companies.
Drug and dossier development working hand in hand to deliver unrivalled quality.
Our dossier centric approach to drug development fast tracks your product to compliance. By compiling your regulatory dossier in parallel with drug development, we can identify and overcome hurdles, and ultimately save you time.
We also have a number of areas of specialist expertise, including solid state research, bio-availability enhancement and modified release, meaning we can handle even the toughest development challenges.