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Non-GMP manufacture of Active Pharmaceutical Ingredients
We can support the evaluation and screening of new chemical entities, through to prime candidate selection, followed by manufacture of the API under Non-GMP conditions, and develop aseptic and non-aseptic manufacture processes.
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GMP manufacture of Pharmaceutical IMP batches
Our expertise spans a wide range of dosage forms and in-house capabilities range from complex transdermal and injectable products to semi-solids and gels.
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Drug Candidate Synthesis
Our expertise in computational chemistry, synthetic chemistry and biological evaluation allow us to provide a full spectrum of services in drug discovery, from pharmacophore design to hit identification, lead optimisation, ADME and drug candidate synthesis and develop aseptic or non-aseptic GMP manufacturing processes for technology transfer.
Clinical trials
We have supported several projects with a seamless transition from our GMP facility to clinics, handling all aspects of the supply chain to enable human studies to be undertaken rapidly, efficiently and cost-effectively, via our FDA and European authority audited partner clinical research centre based in the Middle East.
Our GMP services are currently provided via our affiliate companies in the UK and Europe.
All R&D and drug discovery is provided from our laboratories in Loughborough in the UK.