SME support to evaluate innovative medical technologies: round 5

Key Features

UK registered SMEs can apply for a share of £1.5 million to support the evaluation of innovative medical devices, diagnostics and regulated digital health products.

Programme:     Innovate UK

Award:     Share of up to £1.5 million

Opens: 30th Sep 2019

Closes: 11th Dec 2019

! This scheme is now closed

Overview

The Office for Life Sciences (OLS) will work with Innovate UK, part of UK Research and Innovation, to invest up to £1.5 million in innovation projects. These will support developers of innovative medical devices, diagnostics and regulated digital technology to evaluate their product in a real world clinical setting.

Scope

This competition is aimed at SMEs that have developed and manufactured innovative medical devices, diagnostics or regulated digital healthcare products.

The competition will support the development or design of plans for the collection of clinical data in a real-world setting, and also support the running of these studies.

Your proposal must:

  • describe the innovative or CE-marked device
  • show how your product is likely to have a significant impact, including increasing patient access to innovative technologies where appropriate
  • demonstrate how the product meets the priority needs, such as those reviewed in the NHS Long Term Plan
  • provide evidence that you are working with appropriate stakeholders including NICE, NHS, NIHR and AHSNs
  • outline how your study will allow NICE to evaluate the data you collect

Your project must:

  • focus on understanding evidence gaps and testing product performance to explain the operational impact of your product on the NHS
  • add data to the evidence base that can contribute to the health technology appraisal process, for instance by comparing the use of the new product with the current standard of care
  • involve potential breakthrough technologies
  • help improve methods and systems

Priority will be given to projects that are related to:

  • ageing well
  • cancer
  • digital transformation
  • learning disabilities and autism
  • mental health
  • personalised care
  • prevention
  • primary care
  • starting well
  • stroke
  • workforce

Eligibility

To lead a project or work alone you must:

  • be a UK registered SME
  • carry out your project within the NHS
  • have a product that is aligned with at least one of the NHS’s priority healthcare areas, such as those reviewed in the NHS Long Term Plan
  • have a product that is already available for the NHS to purchase, but that has been marketed in the UK for less than 5 years
  • outline relevant discussions you have had with the main stakeholders, such as the National Institute for Health Research (NIHR), National Institute for Health and Care Excellence and Academic Health Science Networks (AHSNs), to demonstrate the feasibility of your proposal
  • have gained a CE marking for your product

SMEs can work alone or in collaboration with other businesses or research organisations as non-grant claiming partners or subcontractors. Only the project lead will be eligible to claim grant funding.

Funding Costs

Up to £1.5 million has been allocated to fund projects in this competition.

You can choose from 2 options:

  1. Planning and preparation for a study, for which total eligible project costs can be up to £100,000.
  2. A study to collect clinical performance and cost-effectiveness data, for which total project costs can be up to £500,000.

You can apply for funding of up to 50% of the total eligible project costs. Therefore, option 1 applications can claim a grant of up to £50,000. Option 2 applications can claim a grant of up to £250,000.

Projects must start by 1 May 2020 and must be completed by the end of April 2021.

Projects must have a total duration of between 3 and 12 months.

Exclusions

Projects will not be eligible for funding if they involve:

  • CE marked products that are not currently available to the NHS or have been marketed in the UK for more than 5 years
  • medical devices and diagnostics that do not focus on priority areas for the NHS
  • digital health products not regulated as a medical device
  • projects containing any cost for materials or capital usage as part of the application