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