FCS Associates

Health Technology Regulatory and Innovation Programme

The programme will support SMEs that rely on external expertise to commercialise new products, or re-register existing products in-line with new regulatory requirements.

The aim of this programme is to support small and medium-sized companies (SMEs) that are currently producing or are developing products in the medical technology (MedTech), health technology (HealthTech), diagnostics (including in-vitro diagnostics) and software as a medical device markets to access regulatory related advice and support. This is currently very pertinent as the UK and the EU have seen changes to medical device and in vitro diagnostic device regulations which will affect the UK industry. This project seeks to offer support to the UK health technology industry to mitigate these changes.

Companies can apply for grant funding for regulatory support up to £30,000. Regulatory support may include but is not limited to activities such as:

  • Global registrations
  • Mock audits
  • Quality
  • Clinical guidance pertaining to regulatory affairs
  • Technical guidance relating to standards
  • Guidance on MDR, IVDR, FDA
  • Advice on reimbursement models
  • Guidance on Technical File development
  • Contributions towards remedial action (for example electrical safety testing, biocompatibility testing etc)
  • Notified body costs.

Other activities may be funded. If you are unsure if your activity qualifies then please contact the Health Technology Regulatory and Innovation Programme project support team.

Click here to find out more.

Location: UK

Value: £30k

Deadline: 31 May 2022

Date Added: 24 Mar 2022

Our success rate

Need help applying for this grant?

Yes, Please help me write a winning applicationNo, just keep me up-to-date with the latest grants
Twitter Twitter Feed @FCSAssociates
  • RT @Veitchie: I'll be honest, take up for our Fearless Finances workshop is low. I get it, we avoid ££ because delivery is so important, es…
Twitter LinkedIn YouTube
Health Technology Regulatory and Innovation Programme - FCS Associates

Health Technology Regulatory and Innovation Programme

The programme will support SMEs that rely on external expertise to commercialise new products, or re-register existing products in-line with new regulatory requirements.

The aim of this programme is to support small and medium-sized companies (SMEs) that are currently producing or are developing products in the medical technology (MedTech), health technology (HealthTech), diagnostics (including in-vitro diagnostics) and software as a medical device markets to access regulatory related advice and support. This is currently very pertinent as the UK and the EU have seen changes to medical device and in vitro diagnostic device regulations which will affect the UK industry. This project seeks to offer support to the UK health technology industry to mitigate these changes.

Companies can apply for grant funding for regulatory support up to £30,000. Regulatory support may include but is not limited to activities such as:

  • Global registrations
  • Mock audits
  • Quality
  • Clinical guidance pertaining to regulatory affairs
  • Technical guidance relating to standards
  • Guidance on MDR, IVDR, FDA
  • Advice on reimbursement models
  • Guidance on Technical File development
  • Contributions towards remedial action (for example electrical safety testing, biocompatibility testing etc)
  • Notified body costs.

Other activities may be funded. If you are unsure if your activity qualifies then please contact the Health Technology Regulatory and Innovation Programme project support team.

Click here to find out more.

Location: UK

Value: £30k

Deadline: 31 May 2022

Date Added: 24 Mar 2022

Our success rate

Need help applying for this grant?

Yes, Please help me write a winning applicationNo, just keep me up-to-date with the latest grants