VerIQ is a full-service provider of clinical trial services for orthopaedic devices and therapies spanning feasibility, regulatory path planning study design, clinical study execution and market adoption.
We offer a high level of engagement from investigators from network of leading surgeons and internally recognised high-volume sites in the UK. We have a track record of accelerated study set-up and patient recruitment delivering high quality data for complex and innovative orthopaedic trials.
VerIQ has expertise to manage all clinical operations from identifying appropriate patient populations, developing study protocols designed to optimize study success in accelerated timelines, regulatory and ethics submissions, site selection, set-up, recruitment, project and data management and close-out.
VerIQ provides comprehensive support across the full clinical development pathway — from early feasibility through to post-market evaluation. Our model combines operational excellence with academic insight and regulatory expertise.
VerIQ’s partnership model ensures prioritisation, quality, and speed - delivering studies significantly faster and at lower cost than comparable programmes in the US.
Full project delivery including contracting, site coordination, recruitment, and data management through our pre-primed UK network.
Guidance aligned with MHRA, MDR, and FDA requirements to ensure smooth approval pathways for UK, EU, and US markets.
Demonstrating cost-effectiveness and clinical value to support adoption into healthcare systems such as the NHS.
Long-term evidence generation to support real-world performance and compliance.
Get in touch to find out more about how we can help design and deliver clinical studies tailored for better outcomes, higher data quality, and faster execution.
Get in touch to find out more about how we can help deliver studies significantly faster and at lower cost than comparable programmes in the US.
Get in touch