Comprehensive clinical support, scoped to your study.
We offer a full range of flexible, contract clinical operation and CRA solutions to the pharmaceutical, biotechnology and medical device industry — take everything, or just the part you need.
Feasibility & pre-study
We use our expertise and industry-specific tools to determine the feasibility of your clinical trial, then handle pre-study preparations such as ethics submissions and site initiation planning.
- Site feasibility assessment
- Pre-study preparation
- Investigator & launch meetings
- Initiation planning
Ethics submissions & regulatory
Extensive experience handling UK & Ireland ethics submissions for clinical trials — including NRES-compliant patient information sheet and consent form adaptation, and NIHR applications to the NHS Portfolio.
- UK & Ireland ethics submissions
- NRES-compliant documentation
- NIHR / NHS Portfolio applications
Clinical monitoring & CRA support
Our highly experienced CRAs conduct all necessary site visits — pre-study, initiation, interim monitoring and closeout — on-site and remote, with minimal management overhead. We review informed-consent procedures and protocol compliance to ensure good site performance.
- Routine site visits
- Source data verification
- Consent & compliance review
- Remote monitoring
Trial management & line management
Project operations and line-management support for the full duration of the clinical trial process, keeping sites, timelines and sponsors aligned from initiation through to closeout.
- Clinical project operations
- Line management
- Timeline & site oversight
- Sponsor reporting
Closeout
Orderly, efficient site closeout and handover — with documentation reconciled and ready for audit and regulatory submission.
- Site closeout visits
- Documentation reconciliation
- Audit-ready handover
IMP & medical device studies
Specialist support for studies involving investigational medicinal products and medical devices, applying the same rigour across the full study lifecycle.
- IMP studies
- Medical device studies
- Protocol-to-closeout support
Not sure which pieces you need?
Tell us about your protocol and timelines — we'll recommend the right level of support and give you a straight answer on cost and pace.
Start a conversation