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Trial design

Turn complexity into clarity with a tailored trial design approach.

Design smarter, more efficient trials.

Get data-driven insights and expert support

Effective trial design is the foundation of a successful clinical trial. We work with you to maximise the value of real-world data and electronic health records.

Whether you are conducting early-phase research, large-scale trials or post-market studies, we provide data-driven insights and expert support to help streamline trial execution and improve participant recruitment.

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Why partner with us?

Support for faster, compliant, patient-focused trials

Connect to rich real-world data for faster, smarter trial design

Achieve smarter recruitment, cleaner data and faster trials

End-to-end collaboration

Our comprehensive trial planning supports protocol development, feasibility assessments, dataset structuring and ethics approvals. We help make sure studies are designed for maximum efficiency and compliance.

We also offer expert insights into adaptive and decentralised trial design, helping to optimise site selection and integrate hybrid or decentralised trial models for more efficient, patient-centric studies. Plus, our regulatory and compliance expertise supports you to make sure your studies meet regulatory guidelines, reducing delays in submissions.

Unrivalled NHS and academic networks

We unlock access to rich NHS data and outstanding clinical expertise through established connections with NHS research networks, GPs and clinical sites. We help mobilise studies faster and ensure broad patient representation.

Using EHR-enabled analytics, we help refine study parameters by identifying eligible patient populations before recruitment even begins – and that means smarter trial design for you. We also collaborate with leading research institutions, universities and ethics committees to ensure scientific rigor and regulatory alignment.

Seamless implementation and execution

Our advanced FARSITE platform unlocks real-time feasibility assessments, targeted recruitment and improved trial enrolment efficiency. Our secure electronic data capture system, ConneXon, gives you access to high-quality data collection, real-time safety monitoring and compliance with Good Clinical Practice guidelines.

We deliver speed and scalability too, with our integrated digital infrastructure supporting trials at regional, national and international scales, accelerating study start-up and execution.

The smarter, more efficient route to real-world impact

Ready to optimise your trial design?

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“I think one of the strengths of the NWEH team is their responsiveness, they are very knowledgeable in their respective fields and always had the right internal experts on each call. I have already recommended NWEH and will continue to do so.”

Project Manager

Trial Sponsor, January 2025

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NWEH excited to announce a new pilot initiative with CPRD

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Talk to NWEH about your trial design

Discover more. Deliver better.

Get in touch today