European leader in analytical sciences
Quality Assistance S.A. 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.
We assist our clients from candidate selection, through non-clinical and clinical studies, to marketing authorisation, using our state-of-the-art, product-dedicated expertise in analytical sciences.
For each customer and each project, we design customised solutions, define analytical protocols, develop and validate specific new analytical methods and perform characterisation, stability, pharmacokinetic, biomarker and immunogenicity studies as well as batch release testing, in order to evaluate the Quality, Safety and Efficacy of the given drugs.
Quality Assistance S.A. is an expert for the development of
Advanced Therapy Medicinal Products (Cell-Based MPs and Gene Therapy MPs)
Biologics (monoclonal antibodies, ADCs, recombinant proteins and peptides)
New Chemical Entities (e.g. protein kinase inhibitors, synthetic peptides, cytotoxics)
Vaccines (recombinant protein vaccines, synthetic peptide vaccines)
The company holds a unique position on the market with
All its laboratories on one site
180 highly qualified professionals
Over 35 years’ expertise at the forefront of analytical sciences
Our core competencies are
Development and validation of analytical methods
Batch (release) testing
Development and validation of bioanalytical methods
The Quality Assistance environment is GMP, GLP and GCLP/GCP compliant.
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