We successfully design and implement clinical research programmes across all phases of development, from first-in-man studies, to interpreting and presenting data from Phase 4 studies. See our client solutions, or view some case studies.

What we do

Protocol Design & Feasibility

Protocol development assistance and study feasibility assessments.

Consultation on study designs, endpoints, objectives, assessments and statistical analyses, as well as working to identify possible sites and understand the feasibility of conducting the study.

Full Life Cycle Strategy

Full life cycle support, including pre-clinical, clinical and regulatory strategies.

Development of strategies to support new indications or label extensions, obtain or expand market access and support product differentiation and positioning.

Study Start-Up

Creating efficiencies in the initiation of new studies.

Site identification, selection and contracting, regulatory and ethics submission, essential document management and patient recruitment.

Clinical Trial Management

Provision of project and data management for study conduct.

Complete audit-ready clinical study solution which delivers study efficiency, data quality, and patient compliance.

Medical Management and Oversight

Provision of medical expertise to support study design and conduct.

Therapy area and protocol training, development and delivery of medical monitoring solutions.

Clinical Pharmacology

Early phase clinical research strategy development.

Clinical Pharmacology Strategy development, including design and conduct across the spectrum of early phase studies.


Development of publication and communication strategies.

Interpretation of study results, development of publication plans, and execution against those plans to maximise reach of study communications.

View case studies

Contact us today to discuss your project – call +44 (0) 1494 957366