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| Funder | Vinnova |
|---|---|
| Recipient Organization | Draghjälp Ab |
| Country | Sweden |
| Start Date | Aug 01, 2023 |
| End Date | Apr 01, 2024 |
| Duration | 244 days |
| Number of Grantees | 1 |
| Roles | Principal Investigator |
| Data Source | Swedish Research Council |
| Grant ID | 2023-01606_Vinnova |
Purpose and goal: - Mapped regulatory pathway into non-EU countries: UK, Switzerland, USA and Canada. - Created stronger market understanding for UK&I Expected results and effects:
- Mapping of needs and regulatory eligibility requirements in Great Britain has resulted in establishment of Njord Medtech Ltd in 2024
- Mapping of regulatory eligibility requirements in Switzerland has resulted in establishment in 2024 via CH-Rep MedEnvoy - Mapping of regulatory eligibility requirements in the USA and Canada completed, no decision taken yet. Approach and implementation: ** Denna text är maskinöversatt ** Commercial market analysis in the UK was carried out by an on-site consultant who has worked in the NHS for +30-years.
Regulatory mapping of Atle 180 introduction in England, Switzerland, USA, Canada was carried out by experienced QA&RA consultant based in Sweden
Draghjälp Ab
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