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Clinical Research, Commercial Consulting & Global Distribution

Explore what we offer

Clinical Research

We specialise in managing medical device and pharma studies, whether to support regulatory approval or to gather real world evidence as part of PMCF plans as requested by EU or UK medical device regulations. We provide tailored quotes and deliverable based payment systems, as well as our fixed-price support packages.

Commercial Services

We provide specialist end-to-end support to accelerate the commercial success of your products to your target customers. Using the UK as a springboard for global expansion, our experience and expertise can accelerate your growth.

Global Distribution

We support market entry and product adoption through well-aligned, scalable distribution models — tailored to the needs of hospitals, private clinics, and diagnostic providers.

We combine in house clinical research, market access, sales and marketing teams to accelerate market entry and commercialisation of your medical devices and pharma products.

We believe in honesty, simplicity, and going the extra mile, ensuring that your path to market is not only smooth but also successful.

From day one we’ve been passionate about understanding the unique needs of each business we work with. We see ourselves as your partner, collaborating closely with you to help you reach your full potential. Our dedicated teams will support every stage of your journey.

Who we are

Book a call with us

We work with MedTech and BioPharma teams to accelerate clinical, regulatory, and commercial progress. If you're planning a study, preparing for market entry, or need focused support — we’re here to help.

Book an Introductory Consultation to tell us more about your project and explore how we can support your journey.

No pressure. Just a conversation with people who understand the challenges and can offer a clear path forward.


Who We Work With

Short-Term Support Packages

Our fixed-fee clinical and commercial support packages designed to help MedTech and BioPharma companies accelerate market access and adoption.

We understand that not every project needs a full-scale consultancy. That’s why we’ve developed a range of short-term support packages designed to help you navigate specific challenges with speed and clarity.

Whether you're preparing for market access, planning a product launch, or gathering critical clinical insights, our expert-led packages provide targeted support across regulatory, commercial, and clinical domains. Ideal for internal teams needing extra capacity or specialist input, our packages deliver high-impact results without long-term commitment.

Contact Us

Interested in working together? Fill out some info and we will be in touch shortly. We can’t wait to hear from you!

  • “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