# RMS02 - Risk Management System Capabilities and Processes Details of the RMS system capabilities: * Detail or upload a document detailing how known and foreseeable risks are recorded and updated throughout the AI system's lifecycle, including post-market. * Detail or upload a document detailing how risks are estimated and evaluated; this estimation and evaluation must consider when the AI system is used for its intended purpose as well as under conditions of reasonably foreseeable misuse. * Detail or upload a document detailing how other possibly arising risks are evaluated based on the analysis of data gathered from the post-market monitoring system --- # 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/rms02-risk-management-system-capabilities-and-processes.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.