Our Clinical Services department delivers agile, high-quality clinical studies and trials, supporting the TOGL group of companies and selected partners. With a team that is experienced, energetic, and solutions-driven, we specialise in designing and managing studies that are both innovative and effective.
We work primarily in partnership with the NHS, spanning both secondary care and community healthcare environments. At any one time, we manage multiple active studies, from small proof-of-concept cohorts (45+) to large-scale multi-centre verification and validation studies (6,000+).
Our approach is fully collaborative, with our team actively involved in every stage: study design, ethics approvals, deployment, data gathering, and study management.
Unlike traditional CROs, we focus on work within the TOGL organisation and only engage externally through established, mutually beneficial collaborations.
The Clinical Services team provides end-to-end support across the full lifecycle of clinical research, including:
- Protocol design, preparation, and production
- CI / PI identification, selection, and qualification
- REC preparations, submissions, and management
- Material preparation, including CRFs and eCRFs
- Quality and regulatory compliance to required standards
- Public and Patient Involvement and Engagement (PPIE)
- Patient pathway optimisation for effective cohort selection
- R&D negotiation and cost management
- Insurance procurement and reporting
- Study logistics and biobank management
- AE and SAE reporting and management
- Human resource procurement, costing, and management
- Clinical data collection, monitoring, evaluation, and presentation
- Study closures and reporting