Accelerating MedTech success through clinical and commercial expertise.
Explore what we offer
Clinical Research
We specialise in managing medical device 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.
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.
Support Packages
We offer clinical and commercial support packages for MedTech companies looking to enter and scale in the UK market. From clinical trial setup to market access and commercial strategy, our expert-led services help accelerate product adoption and healthcare impact.
Schedule a chat with us
We would love to hear more about your MedTech and support your journey. Why not schedule a Free Consultation with us.
We combine in house clinical research, market access, sales and marketing teams to accelerate market entry and commercialisation of your medical devices and 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
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Rescue Package
A fixed-fee service to get clinical trials back on track. We assess documentation, recruitment status, and gather KOL feedback before recommending realistic, risk-managed steps for improved trial delivery.
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Multi-Disciplinary Starter Package
Ideal for early-stage MedTech companies, this package offers integrated clinical, market access and commercial expertise for one fixed fee. Supports in-house teams with evidence planning and GTM strategy.
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Clinical Research UK Site Selection
We identify and assess UK sites using therapeutic expertise and local relationships. Includes feasibility surveys and site visits to keep study setup moving despite internal resourcing gaps.
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Clinical Study Set Up
Comprehensive support to move from protocol to activation. Includes clinical documentation, regulatory submissions, site contracts and start-up coordination using local know-how and SOPs.
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Investor MedTech Evaluation
This package supports investor due diligence by reviewing the clinical, regulatory and commercial strategy of your MedTech asset. It includes a SWOT analysis, health economics review, GTM plan, and a regulatory roadmap to assess readiness.
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Site Selection Visit Package
Where sites are already identified, we provide support using MediLife SOPs and trained CRAs. Ensures smooth, compliant site visits and project continuity while internal resources scale up.
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UK Ethics Application
We guide your medical device study through UK ethics approval using your trial documentation. This includes a full review of materials and submission via our standardised SOPs to minimise delays.
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UK Regulatory Submission Package
We prepare and submit your MHRA application for a UK medical device study. Our experts ensure your documentation is fully compliant and the submission process is handled efficiently under MediLife SOPs.
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More Packages
Explore our full range of support packages including: Clinical Operations, Market Access, Market Quantification, Value and Brand Positioning, KOL Engagement Commercial Strategy and more.
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!