We can support our clients right through their project life cycle, from early project design (including professional and patient involvement), to inception and through the governance processes, enabling studies to be quickly set up and run with support in place.
We have an established track record of rapid feasibility, good recruitment, and high data-quality collection. After your study has closed, we can provide support for data analysis write-up and further regulatory submissions. We work with customers of all sizes, maturity, and development stages. Even if you have never undertaken a clinical research project before, we can provide the advice and guidance you need to navigate the clinical research landscape.
We provide all customers with high-quality, customised services, ensuring that studies are conducted to regulatory standards and remain aligned with project objectives and milestones. We have robust quality assurance systems in place and can host audit and monitoring teams for sponsors and regulatory authorities. We can also provide access to a broad range of bioanalytical services.
Planning and Set Up
- Study design
- Feasibility assessment
- Protocol writing
- Ethics submission
- MHRA clinical trial authorisation
Study support
- Data management
- Study monitoring
- Laboratory sample analysis
- Pharmacy services
- Study recruitment
- Study conduct
Post-study
- Statistical Analysis
- Report writing
- Archiving
- Regulatory submission