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Clinical trial experience, Phase 1 to Phase 4.

Experience across complex, multinational trials.

Founder track record

19 years

of clinical trial delivery

Global

start-up experience across the UK, Europe, the Americas, Africa, the Middle East and Asia-Pacific

32 UK sites

activated in 10 weeks

11 years

in study start-up and site activation

Scientist preparing a laboratory study sample

Phases

Phase 1 to Phase 4, interventional and non-interventional.

Therapeutic areas

Oncology, haemato-oncology, rare diseases, respiratory, inflammation, cardiovascular and paediatrics, with experience in ATMP and gene therapy studies, including GMO trial applications.

Regulatory frameworks

ICH E6(R3), EU CTR 536/2014 and CTIS, MHRA, HRA and Research Ethics Committees, HPRA and NREC-CT submissions in Ireland.

Systems

EDC, eTMF, CTMS, IRT and eCOA platforms.