Clinical Services

We specialise in the strategic design and delivery of clinical trials for MedTech and Biotech companies.

We believe clinical research should do more than satisfy regulatory requirements — it should generate meaningful evidence that drives real-world adoption and supports faster market access.

Our UK-based team works globally to design and implement studies that meet regulatory standards while aligning with your commercial goals. Whether you need support with regulatory submissions, PMCF activities, or real-world evidence generation, we provide a flexible, high-integrity framework built for MedTech innovation.

We combine regulatory clarity, scientific rigour, and commercial understanding to help you bring your product to patients — faster, and with confidence.

You bring the innovation. We bring the structure to support it.

How we work

  • Short-term packages or long-term partnerships

  • Milestone-based payments with transparent pricing

  • End-to-end project management, from ethics to close-out

  • Effective trial implementation and deliveryRisk-based monitoring and dedicated CRA support

  • Experience in decentralised and diverse trials

  • Evidence generation aligned to clinical practice and market access

What we offer

  • Cost effective, transparent pricing

  • Effective trial implementation

  • Regulatory applications & project management

  • Risk based monitoring & CRA outsourcing

  • Network of trusted partners to provide support in the USA, Primary Care & at home nursing

  • Real world evidence & de-centralised trials

  • Linked to market adoption & clinical practice

Download our free guide:

How to Budget for a Clinical Study.

Case Study

Rescuing an Underperfoming Clinical Trial

In 2023, MediLife was approached by one of our partners regarding a clinical trial that was struggling with recruitment, budget overruns, and operational inefficiencies.

This case study outlines how MediLife's intervention helped transform the study's performance.

27% increase in recruitment

Boost in Principal Investigator engagement

Increased commercial sales

  • “Working with MediLife was a very positive experience - they were always very helpful and on hand if matters arose, which is the most important thing from both a CI and PI perspective.”

    Chief Investigator

  • "MediLife has provided sage advice and followed up with timely and smart coordination to enable quick completion of objectives and action items relating to clinical study activities (site qualification, site contracting, site approvals, government approvals, site initiation)."

    US Custom Made Device Manufacturer

  • “We started working with Ian and his team at MediLife in 2019 and they have been instrumental in enabling us to successfully launch our products. They have supported us with many key areas of our business including initial development of our Global strategy, UK regulations, managing our clinical study, supply chain distribution & logistics as well as providing us with a sales team and Global marketeer to support our product launches. The MediLife team have also helped us to develop and improve our products based on valuable customer feedback they have captured. Suffice to say, we have built a strong partnership with MediLife, one which I hope to see continue for many years to come.”

    CEO, Swedish MedTech