Our dedicated Phase I clinical trial site is designed with participant safety and trial efficiency as priorities. We have created a comprehensive, self-contained facility with everything required for a seamless and safe trial experience: two ward areas for overnight stays with a volunteer kitchen and recreational space; round-the-clock coverage by the hospital’s medical emergency team. Our onsite, MHRA-licensed GMP manufacturing suite that enables us to produce, release and dose IMPs under one roof; and an onsite pharmacy and gamma-camera imaging suite.
We deliver the full spectrum of early-phase clinical trials, including First-in-Human; single- and multiple-ascending dose (SAD/MAD); bioequivalence and bioavailability; food-effect; adaptive; pharmacokinetic; and drug–drug interaction studies. Our experienced team of physicians, nurses, clinical trial associates and pharmacy staff ensures the safe and efficient running of your study. All site conduct staff are trained to a minimum of Immediate Life Support (ILS).