Our CDMO services & facilities

We offer end-to-end services and experienced support from pre-clinical to commercialization, from your idea to the market.

R&D and preclinical

Pre-formulation activities
Feasibility studies
Non-Clinical batches manufacturing
High-throughput formulation screening capacities
ICH compliant stability testing

Clinical phases

Clinical trial batches manufacturing (Phases I, II, III)
Analytic method development & validation

Commercial

Project Management
Financial optimisation upon request
EU & US Regulatory compliance and filing
ICH compliance
Packaging
Logistics

Innovation

Tailor-made equipment, technologies, infrastructure and services, and more than 20 years of expertise all in 2 GMP approved environmentally friendly facilities in Liège, Belgium.

Flexibility

Tailored approach to fit every project, with flexible business models and agile capacities including grade C and D clean rooms accredited for multi-product manufacturing.

Efficiency

Quick onboarding, high-throughput formulation screening, easy scale-up, and end-to-end or fee for service approaches, to ensure the most efficient road to success.

Expertise

Each project is embraced and supported by reliable, committed and highly-skilled talents. With a genuine sense of dedication, our teams become your team, working towards your goals.

Support

Legal, finance and business development talents provide you with experienced support and flair to seize the best opportunities throughout every program, from R&D to commercial manufacturing.