# RMS05 - Residual Risks The risk management measures shall be such that any residual risk associated with each hazard, as well as the overall residual risk of the AI application, is judged acceptable, provided that the AI application is used in accordance with its intended purpose or under conditions of reasonably foreseeable misuse. Those residual risks shall be communicated to the user. * Record or upload a document recording the assessment of each of the residual risks and whether they are considered acceptable. Also, record an assessment of the overall residual risk and whether that is considered acceptable. * Record or upload a document recording how the residual risks are or will be communicated to the users. --- # Agent Instructions: Querying This Documentation If you need additional information that is not directly available in this page, you can query the documentation dynamically by asking a question. Perform an HTTP GET request on the current page URL with the `ask` query parameter: ``` GET https://documentations.seclea.com/fda-ai-based-samd/risk-management-system-rms/rms05-residual-risks.md?ask= ``` The question should be specific, self-contained, and written in natural language. The response will contain a direct answer to the question and relevant excerpts and sources from the documentation. Use this mechanism when the answer is not explicitly present in the current page, you need clarification or additional context, or you want to retrieve related documentation sections.