Health Authority Correspondence, Tracked to Closed
Assyro RIM is regulatory information management (RIM) software for planning and tracking submissions, health authority correspondence and commitments, part of the Assyro AI compliance platform. Drop in an agency letter and Assyro reads its type, authority, dates, and stated deadline, then routes it: questions to a response workspace, meetings to dated milestones, and informational letters to the file.
Agency Correspondence Without the Inbox Hunt
Assyro RIM keeps every letter, meeting, call, and email with a health authority in one record, worked to closed.
One Way In for Every Letter
Drop a letter and Assyro reads its type, authority, application, letter date, and stated deadline, each with the page it came from. Your team confirms the details before anything is saved.
Routed by What the Letter Asks
Letters that need an answer, such as information requests, open a response workspace with each question listed. Meeting requests become a meeting record. Acknowledgements are filed with no due date.
Meeting Milestones From FDA's Timelines
For FDA Type A, B, C, D, and INTERACT meetings, Assyro dates the request answer, package, preliminary responses, and minutes from FDA's formal meetings guidance, and recomputes them when the meeting date moves.
A Log an Inspector Can Use
Original files are kept unchanged with their SHA-256 hash, and a file attached by mistake is withdrawn, never deleted. Export the log as CSV or PDF with the audit trail.
Deadlines From the Letter, Not From Memory
A due date comes from the deadline the letter states, from the type's published timeline, or from your team. Informational letters get none.
Unchanged Originals and a Full Audit Trail
Each original file is stored with its SHA-256 hash and never altered, and every change to a record is written to the audit trail.
Every Product's Correspondence in One View
Filter by product, application, authority, owner, or due date, with related items grouped into threads.
Guides for your next decision
Explore requirements, compare workflows, and prepare your evaluation.
Questions About Health Authority Correspondence Software
Practical questions regulatory teams ask about logging and tracking correspondence with FDA, EMA, Health Canada, and other authorities.
