We provide all the functions of a fully resourced pharma/biotech company, often providing ‘bolt-on’ services that complement a client’s in-house resource, enabling them to access all the development capability required at each stage of their project.
Founded in 2001, we’ve spent more than two decades expanding our service offering, growing steadily in geographical reach to become an established world-class global CRO, backed by an experienced team of over 900 associates.
Our experts review data for regulatory acceptability and advise on development strategies
We advise on requirements and liaise with third-party toxicology providers
We identify relevant academic units and personnel for early-stage advice
Employment of a pragmatic and experienced qualified person (QP) who will:
Location of high-quality GMP units, particularly those able to produce special batch sizes
Liaison with clinical trials supplies management units, importers and distributors
Management of import and QP release of investigational and marketed drugs in the EU and other territories
Our team is ready and willing to support your non-clinical needs.
To discuss your specific project requirements, contact us today.
