Our Network

Together with PRO RETINA Deutschland e. V., Retina Suisse, and Retina International, we advance education and care. This collaboration increases reach, user-friendliness, and everyday support. Specifically, this means: We link medical content with accessible information resources, support information events and webinars, and promote the exchange of experiences among patients, relatives, and healthcare professionals.
For people with RP, reliable guidance is crucial. Therefore, we closely coordinate content (e.g., on therapy eligibility, application, follow-up examinations, and reimbursement options) with our partners. Additionally, we support peer offerings – such as self-help groups, mentoring, or digital consultation hours – so that information is not only accurate but also accessible and practical for everyday life. The community also provides us with valuable feedback on instructions, accessories, and service processes. This feedback is incorporated into our product maintenance and training materials.

Currently, long-term data are being collected in Germany as part of a G-BA evaluation study – at 17 university and specialized clinics. Close collaboration with clinics in Germany and Switzerland strengthens both care and evidence.
Our collaborations include, among others: indication assessment and prescription in specialist practice, standardized training with individual parameter settings, and regular follow-up examinations with defined outcome measures. Study centers support data quality (standardized test procedures, documentation) and continuing education for practice teams.
This structure creates continuous knowledge transfer: Findings from clinical research – for example, on dosage questions, safety, and ease of use – are transferred into clinical practice. Conversely, real-world data from care help refine study hypotheses and drive improvements in application, accessories, and patient information.