Texcell is your international, world-class provider of pharmaceutical and biotechnology services, performed in full compliance with GLP and GMP standards, for the development and testing of biotherapeutics. Texcell’s offers a diverse portfolio of viral safety, immunology, cell culture, and laboratory services.
Since 1987, thanks to our vast experience and expertise, Texcell has provided data supporting a large number of products now licensed by the FDA, the EMEA and the MHW. We have extensive experience with a diverse range of molecules including recombinant proteins, monoclonal antibodies, vaccines, gene and cell therapy products, medical devices, and other products of human or animal origin such as blood-derived products, heparin, hyaluronic acid and collagen.
Capitalize on our expertise to significantly reduce the costs of your drug development efforts and minimize the timeline for your drug to reach the clinic. Explore our website to identify useful services and protocols that we offer in biosafety testing, virus and prion validation, immunoprofiling, and cell development
Our top priority is achievement of your goals:
- Customer satisfaction: today, the development time for a new molecule has to be as short as possible. Viral safety testing, viral clearance study and clinical studies need to be continually improved in order to optimize therapeutic strategies.
- Provision of the best services: Texcell mobilizes the people, protocols and tools needed to complete your project successfully.
- Guaranteed timelines: your dedicated project manager will provide a weekly progress report.
- Guaranteed quality: our quality department audits each study according GLP and GMP – Regulatory Agencies (AFSSAPS) and our clients audit our finality system regularly.