Existing methods for risk assessment for medical aids are being surpassed by the rapid rise and availability of apps, serious games and online e-health applications. There is a lack of transparency for end users (consumers, patients, care professionals and consultants, and health insurers) regarding the status, operation and effectiveness of these new tools. At the same time, existing filters for risk assessment of medical aids often lead to excessively strict validation requirements for these new tools, which inhibits their possible contribution to better and more affordable care for the patient. It also erects barriers to new entrepreneurial entrants to the care market and their innovative ideas. This all requires an improved system of risk analysis and validation of e-health applications. A vital condition for an improved system is the introduction of the shortest possible assessment period for this form of quality care, considering the tempo of technological developments in both technical platforms and the applications that run on them (critical time-to-market), so that products do not lose their value before they are released to the market.
