Full transparency on EryonOne's evolutions. Deliveries are dated, work in progress and forecasts too.
A signed final report (timestamped fingerprint) will consolidate all points raised, comments and decisions of a processing run. PDF format with table of contents, suited to internal audit and regulatory submission requirements.
After MDR and ANSM, opening of international frameworks: FDA 21 CFR Part 11 and ISO 13485 for medical devices exported outside the EU. Prioritisation based on community votes.
Suggest a product improvement from the roadmap. Other users will be able to vote for your proposal, and you will be notified by email as soon as it goes into production. Limit of 5 proposals per user to stay focused.
Priority is refocused on the main review flow: better progress tracking, duration estimation and more readable presentation of the points raised.
The "Resend email" button can no longer be used in a loop. The delay increases progressively (60s → 5min → 30min → 2h → 24h), with automatic reset after 24h of inactivity. Atomic database protection against double clicks. The verification waiting page shows the countdown in real time.
The Claude chain is wired server-side with instructions, traceability and usage tracking. Activation outside simulation depends on the production configuration and the Anthropic API key.
A client account can now invite several users. Distinct owner/member roles, shared credit ledger, audit of actions per user.
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Votable suggestions arrive in June 2026. Until then, create your account to follow updates.