With a network spanning six strategic locations across Europe, our facilities are carefully engineered and uniquely built to support and enable early-phase development for our partners' oral drugs, injectables and nanomedicines.
Kleimoer 4, Ghent, Belgium
Kloosterstraat 9, 5349 AB Oss, Netherlands
Tallvägen 6, 151 38 Södertälje, Sweden
Calle Noáin, 1, Noáin, Spain
W.A. Scholtenstraat 7, 9403 AJ Assen, Netherlands
Our headquarters in Ghent is home to specialist expertise and tailored CMC regulatory services engineered to support you from pre-clinical to clinical manufacturing.
At this site our formulation and manufacturing capabilities are focused in injectable drugs, as well as oral drugs, especially those with low solubility challenges.
Our site in Oss is situated on Pivot Park, a reputed Life Sciences campus with a special focus on pharmaceutical innovation in the Netherlands. At Ardena Oss, we focus on drug substance, solid state, and nanomedicines services, including highly potent compounds.
Ardena Södertälje AB has brought dozens of active pharmaceutical ingredients (API) from early lead molecules to clinical studies.
Focusing on small-molecule oral solid drugs, our Pamplona site specializes in highly potent compounds and differentiating technologies including spray drying, from development to clinical manufacturing for early and late phases, as well as commercial manufacturing of niche drugs.
Assen is a highly specialized and innovative facility that offers a full range of bioanalytical services from drug discovery research up to phase IV clinical studies.
Using the right standards at the right development phase, our comprehensive program management services streamline your small molecule drug development.
Helping you turn your compounds that show promise into GMP-grade drug substances.
We advance your clinical candidates through the pipeline quickly and safely with specialist drug product services.
Our bioanalytical platform supports your preclinical and clinical stages with expert testing services.
Our comprehensive CMC regulatory services streamline preparation and submission of your registration file.
Using the right standards at the right development phase, our comprehensive program management services streamline your large molecule drug development.
We advance your large molecule candidates through the pipeline quickly and safely with specialist drug product services.
Our bioanalytical platform supports your large molecule drugs through preclinical and clinical stages with expert testing services.
Our comprehensive CMC regulatory services streamline the preparation and submission of the regulatory files for your large molecule drug.
Using the right standards at the right development phase, our comprehensive program management services streamline your nanomedicine drug development.
We turn your nanomedicine candidates into suitable drugs with specialist development and manufacturing services.
Our bioanalytical platform supports your preclinical and clinical stages with expert testing services.
Our comprehensive CMC regulatory services streamline the preparation and submission of the regulatory files for your nanomedicines.
We have a deep understanding and exceptional experience which we leverage to guide our approach and deliver the best possible outcomes for our partners.
Get in touch to see how we can craft your path to the clinic with dedicated capabilities.