What do you need to do to commercialise a medical device? How long will it take? How much will it cost?
These are questions our Innovation, Commercialisation and Regulatory team are frequently asked.
Medilink have developed the MediPath Innovation Roadmap™ to help our clients plan their innovation journey to reduce risk, accelerate the speed to market, maximise the probability of market success and enhance profitability.
Drawing on our extensive experience and understanding of best practice, our team of experts have created a new tool to ensure that all key activities and milestones are considered. MediPath™ gives a comprehensive breakdown of all commercial, technical, clinical and regulatory actions, along with the associated resources, costs and time to get a medical device to market.
Successful product development is not just about designing and launching a product. There are many more steps involved to ensure that the market opportunity is sufficiently attractive, the device will gain regulatory approval and reimbursement will be achieved. All these stages are critical for successful product commercialisation.
MediPath™ is a flexible seven-step tool that helps you navigate the innovation landscape, designed to ensure that your R&D plans are robust, that the project has the right expertise, and that when requesting investment from public or private funding there is a justification based on real data.
Wherever you are in your journey, it can be used to validate your product development plan, de-risk the following stages and allow you to address deficiencies in your existing processes.
Tailor your roadmap to your device – free consultation
The Innovation, Commercialisation and Regulatory Team are offering a new service in which we walk through the MediPath™ tool, starting from an introductory half-day session to more detailed evaluations and support depending on your needs.
If you would like to discuss any of these stages or to understand how the roadmap can de-risk your innovation and accelerate the speed to market, we are offering a free 30-minute consultation. Contact us on: [email protected]
Patrick Trotter PhD MBA (TechMgmt), Stefanie Lowry BSc, MSc

For more information on each stage, click on the links below:
Testimonials
The Medilink Innovation and Commercialisation and Regulatory course was fantastic with relevant content bespoke to our request for training. The interactive content and innovation management tools will help us manage and optimise our portfolio. The learnings gained from this course have upskilled our entire team. Great course!
Medilink provided us with consultancy services which covered extending the intended purpose and product claims for one of our legacy devices. The work identified key user needs associated with using the device for a new clinical indication and has helped us articulate a series of new claims and has fed into our R&D projects in designing new predictive test methods, identifying the acceptability of the benefit risk ratio from competitor benchmarking and also input into our clinical evidence general plans. We look forward to working with Medilink in the future.
Medilink have authored a number of clinical evaluation reports for our family of class III implantable tissue regenerative products and we have been delighted in the speed and quality of the service and reports, which have also satisfied the notified body. We look forward to continuing our relationship with Medilink
Medilink has been instrumental in helping us navigate complex UK, EU, and US regulations, develop a compelling value proposition, and refine our product labelling and positioning strategy. The Medilink team also provided crucial guidance on planning and understanding the structure, as well as the primary and secondary endpoints, of future clinical trials—insights that will be invaluable for our resource allocation and strategic planning. Furthermore, they identified potential partners through thorough due diligence, assessing gaps in their portfolios and their preferred strategic approaches to growth. Medilink’s contribution has been invaluable in advancing our journey toward commercialization.
The contribution of the Medilink team has helped to establish the resources, costs and timelines for commercialisation, which has been invaluable in our R&D planning. Metlase look forward to working with the Medilink team in the future as the project progresses.”
Medilink conducted a thorough market and competitor assessment regarding the opportunities for ClotProtect’s small molecule to attenuate blood loss. The work was conducted with considerable insight including identifying types of clinical need, which could represent commercial opportunities. The assessment also analysed existing types of solution with their benefits and limitations including clinical risks. The report also included a list of top-level design requirements and an appraisal of how the technology might be differentiated from existing solutions. The work was important for the strategic direction of the formation of the University Spin out – ClotProtect Therapeutics Limited.
Let me first take this opportunity to thank you very much for your contributions over the past 2 years or so. Without this, our business unit would not be what it is today. The work you have completed sets a very high standard.
BioMin Technologies commissioned Medilink to author a Clinical Evaluation Report (CER) for a class IIB device technical file submission with a tight deadline and were delighted with both the quality and speed of the report. In fact, it’s the best overview and review of our product I have seen and we will use it for technical, marketing and other purposes. Many thanks to Medilink on a great job.
Medilink authored a development Clinical Evaluation Report and we were delighted with the quality of the work, it was comprehensive, insightful and also provided us with a much deeper understanding of alternative solutions and competitor products. We look forward to working with Medilink again in the future.
The Medilink Team produced a “lie of the land” assessment for us covering market opportunity, competitor analysis, regulatory and reimbursement considerations. This input has been hugely beneficial and has allowed us to make informed investment decisions and helped de-risk our future pipeline.
Haemoconcepts are developing a novel device and we required a greater understanding and segmentation of the market and a value proposition. Medilink helped us understand the size and value of the market and also prepared a preliminary value proposition that allowed us to understand the key metrics and value that our device can provide the NHS. Thanks, it was a great report.
Medilink produced an excellent commercialisation road map, documenting the product development process with key milestones and the documentation needed for commercial activities to reduce market risk and the technical documentation required for submission to the notified body. The report has provided clarity in the route to market and has allowed us to plan both the time and resources needs for a successful product launch.
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