What we do

What we do

Medtechtomarket offers a comprehensive suite of services for product development, right through from bright idea to launch, promotions and sale.

Medical deviceIdea protection

We work closely with inventors and companies to effectively and economically achieve commercial protection for Intellectual Property (IP), applying for patents and design rights.

Market analysis

We can support you in analysing and evaluating the healthcare economics and business case for your technology, to identify whether there is a market need with an appreciable financial return.

Business planning

With proven success in effective, comprehensive strategy planning, we can help you to deliver. A strong business plan will also help support funding bids and grant applications.

Fundraising

Access funding through our strong links with angel investor networks and VCs, and proven success in grant application.

Medical device twoProduct design and development

Our team of experienced product developers and development scientists provide a full product development service at our facilities in Thornton Science Park, including:
o GLP laboratory product verification and validation, planning and execution
o Diagnostic Instrument and Cartridge feasibility and performance assessments
o Mechanical and electronic design
o Product improvements
o Medical software design and validation

Clinical evaluation

Leverage our knowledge and resources to achieve a more efficient path to market. Medtechtomarket supports clinical trials and evaluation from start to finish. We can develop and design strategy and protocol, manage the studies and data, monitor the trial at every stage, and carry out statistical analysis of results to prepare a full, in-depth report.

Manufacturing

Medtechtomarket has links with manufacturing facilities within the UK, as well as FDA Accredited contract partners in Asia. We guide the process from early manufacture through validation, and scale-up to large-scale commercial manufacturing.

Medical device in useRegulatory submissions

We can support and guide regulatory assessments, roadmap planning, CE marking and FDA 510(K) applications, and other global regulatory submissions as appropriate, to ensure each technology has the best chance possible of launch in the chosen market(s).

Sales and marketing

We have the experience and resource to develop packaging and labelling, user manuals, and launch support materials. We have a large network of distributors, both in Europe and the USA. We can work with you to both appoint and manage distributors.

Exit

With a strong network of industry and healthcare contacts and partners, we can help you to achieve commercial exit, through sale or licensing.