From development to market ABL Europe provides GMP viral vectors, contributing to the success of our clients’ immunotherapy innovations.
ABL Europe SAS is a pure-play GMP CDMO licensed in accordance with EMA, completely dedicated to the provision of viral vector GMP contract manufacturing services, under the corporate ownership of Institut Mérieux. ABL has a strong technical & regulatory track record in process development, scale-up & GMP manufacturing of filterable & non-sterile filterable (aseptic processing) viral vectors used in all phases of clinical development globally. 2 GMP sites provide adherent platforms (< 60 m2) and suspension (< 500 L) capabilities for drug substance, with drug product (< 10,000 vials per batch) in-house, experience in process characterisation and validation, ABL provides its clients with a long-term strategic manufacturing option through clinical development & licensure for a range of viral vector gene therapy & vaccine products. ABL Europe’s clients are located worldwide.