Last updated: May 2026
By accessing and using MedMI ("the Service"), provided by MedMI Technologies Pvt. Ltd., you agree to be bound by these Terms of Use.
MedMI is an AI-assisted documentation tool, NOT a certified medical device or a substitute for professional regulatory review. The Service generates draft Risk Management Files (RMF) based on ISO 14971 principles. However, the Manufacturer assumes full and absolute responsibility for:
You retain all intellectual property rights to the device specifications you input and the final exported RMF documents. MedMI retains all rights to the software platform, algorithms, and templates.
In no event shall MedMI Technologies Pvt. Ltd. be liable for any regulatory audit findings, product recalls, or patient harm resulting from the use of documentation drafted using our software. The tool is provided "as is" without warranty of regulatory compliance.
For questions regarding these Terms of Use, please contact us at contact@medmi.in.