During the project, we propose to:
- Set up clinical research with established European clinical research partner on a per test basis.
- Set up partnership with European clinical partners in ophthalmology, neurology to built up our normative database for developed test.
- Define our regulatory pathway and strategy, including activities and documents needed for regulatory approval.
- Conduct pre-marketing activities, such as analysis of market, qualitative interviews with potential customers, users and distributors, leading to a target product profile.
- Prepare dissemination materials, such as brochures, conference materials, online educational materials and user demonstration material, distributor demonstration materials.
- During project the aim is to find at least one pan-European distributor and one worldwide distributor.