Our state-of-the-art labs support drug substance (API) and drug product (finished product) analytics across all phases of clinical development and into commercial release.
We offer a full suite of Analytical Testing for a range of different product types including small molecules, peptides, biologics, conjugates, potent substances and controlled substances. Our vast pool of scientific knowledge can help to overcome the analytical challenges that typically arise during drug development.
All our analytical laboratories are fully certified by the appropriate authorities (FDA, MHRA, INAB, HPRA). Currently employing ~200 personnel, our global analytical team spread across three sites consists of highly experienced analysts, technicians, project management and quality assurance to ensure that your product is in safe hands.
We offer Method Development & Validation, Pharmaceutical Drug Product Release Testing, Stability Studies of Pharmaceutical Products, Solid State Services, Spectroscopy & Biologics Testing.
In 2017 we opened our purpose-built analytical complex to expand the footprint at our UK headquarters. Employing over 100 analysts, we offer standalone services and to support manufacture of small molecules and peptides, drug substance (API), drug product and clinical trial supply. Our vast pool of scientific knowledge can help overcome the analytical challenges that typically arise during drug development.
Our Physical Sciences group, also located at our Craigavon campus, unites chemists, analysts and formulators in one team, adding value through synergy.
Our state of the art lab based in Athlone, Ireland, offers a comprehensive range of flexible pharmaceutical testing services to support our clients’ drug development programs. The needs of our global client base are met by our experienced team of ~50 personnel adhering to industry regulations including FDA, EMA and PMDA, under GMP standards.
In 2020 we announced an addition to our existing suite of analytical solutions to include biologics testing covering GMP lot release and stability testing, analytical method development / phase-appropriate method validation and raw material testing. Our facility is Ireland’s only GLP accredited bioanalysis lab.
Our GMP analytical development and testing facility, located in Souderton, PA, has doubled its footprint to meet client demand and is fully equipped including housing stability chambers per ICH guidelines.
Our team, comprising of ~30 people, ensure our clients receive an experience that is personalized to their project and their needs. The agility of our lab means we are able to make rapid adjustments to projects scope, successfully complete projects with aggressive timelines, and onboard large projects quickly while maintaining the dedicated time each projects needs and deserves.