Since April 2023, we have achievements in the following three aspects:
REGULATORY COMPLIANCE:
1. We have renovated the International Organization for Standardization (ISO) with a focus on medical devices (13485) on 10th January 2024 (valid starting on 1st April).
TECHNOLOGICAL DEVELOPMENT:
1. We started expanding our software development kit (SDK) to allow third-party applications (e.g. Encevis
https://www.encevis.com/(opens in new window)) to connect to our home-based electroencephalographic acquisition system (Orbit® or Atlas®).
2. In addition, we prototyped the Brainhero Gameshop, a platform for easy and fast game prototyping, testing, and deployment that will allow our patients to train with similar neuroplasticity protocols using different interfaces (i.e. games).
3. We also optimize the ear clip material delivered with our portable EEG (Orbit®) to obtain durable signal acquisition while enhancing more comfort for the patients while training.
CLINICAL INVESTIGATION:
1. We submitted the Clinical Evaluation Plan and the Clinical Evaluation Report for auditing compliance with the MDR 2017/745 (third revision) on 31 January 2024. The answer was delivered on the 4th of March, 2025, encouraging us to start collecting clinical data and expand the intended use of our medical device to specific patient populations. A date for the next revision was suggested for November 2024.
2. In addition, we started the psychometric analysis of clinical symptoms. To date (19 March., 2024), we found that for Autism, 100% of the patients reported 1) a better understanding of cause-effect relationships and 2) Improvements in accepting suggestions and solutions from others (e.g. parents). For Attention/Deficit-Hyperactivity Disorders (ADHD), 100% of the patients reported 1) Enhancement in concentration and 2) a better ability to remember times and locations (e.g. do not lose things)