Quality Assistance is a leading European Contract Research Organisation providing the pharmaceutical industry with all the analytical services required by EMA and FDA regulations for the development and marketing of innovative human medicinal products.
Quality Assistance is an expert for the development of:
- New Biological Entities (monoclonal antibodies, ADCs, proteins)
- New Chemical Entities, oligonucleotides, peptides
- Nanomedicine products
- Cell-Based and Gene Therapy Medicinal Products
In order to evaluate the Quality, Safety and Efficacy of the given drugs for each client project, our skilled teams design customised solutions, define analytical protocols, as well as develop and validate specific new analytical methods. In addition, we perform characterisation, stability, pharmacokinetic, biomarker and immunogenicity studies, and batch release testing.
The Quality Assistance environment is GMP, GLP and GCLP/GCP compliant.
+32 (0) 71 53 47 81