Our expertise in the Pharmaceutical Industry allows us to support our clients throughout the market authorization process, starting from R&D through Clinical Operations, Regulatory Affairs, Engineering, Safety, and Quality. To respond the demands of a growing market, we have established numerous partnerships with companies specializing in gene and cell therapy. We work from user requirements to qualification (equipment, processes and utilities), production and operations and also for production support and continuous improvement.
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industry sector.
Industrie Pharmaceutique & Biotechnologie
Notre expertise dans l’Industrie Pharmaceutique nous permet d’accompagner nos clients tout au long du processus d’obtention d’autorisation de mise sur le marché avec comme point de départ la R&D en passant par les Opérations Cliniques, les Affaires Réglementaires, l’ingénierie, la Safety et la Qualité.
Medical devices
We assist our clients with strategy and regulatory compliance (EU 2017/745 and 746), implementation of a Quality system (ISO 13485), internal and subcontractor audits, clinical trial applications, and clinical report writing for CE marking.
Chemical Industry
Notre expertise en Chimie s’étend de la Biochimie et biomatériaux industriels en passant par la chimie fine et Agrochimie. Nos missions s’articulent autour des études en R&D par la caractérisation des matériaux.
Cosmetics
We provide specialized advice on European regulations, GMP, Quality and risk management, and the implementation of new ISO microbiological standards.

We assist our clients with strategy and regulatory compliance (EU 2017/745 and 746), implementation of a Quality system (ISO 13485), internal and subcontractor audits, clinical trial applications, and clinical report writing for CE marking.
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Our expertise spans from Biochemistry and industrial biomaterials to fine chemicals and Agrochemistry. Our projects include R&D studies, material characterization through chemical and chemical test, polymerization and more.
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We provide specialized advice on European regulations, GMP, Quality and risk management, and the implementation of new ISO microbiological standards.
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