medical-device-postmarket医疗器械上市后监管（Post-Market Surveillance, PMS）实操手册——中美欧日四市场上市后义务对照（不良事件报告、PSUR 定期安全报告、FSCA/召回现场安全纠正、PMCF 上市后临床跟踪）、各市场报告时限与流程清单（美国 21 CFR 803 致死 30 天/严重 90 天、欧盟 MDCG 2022-21 PSUR 频率、中国 2018 年 1 号令报告时限、日本 PMDA）、PMS 计划与 PSUR 撰写框架、监测-报告-纠正闭环落地，附零依赖本地工具一键查询义务对照、报告时限与生成 PMS/PSUR 框架。面向医械法规、质量与临床负责人，拿证后的持续合规一站理清。
Install via ClawdBot CLI:
clawdbot install zhaoxinghua09-cell/medical-device-postmarketLoading skill content… the page will refresh in a moment.
Usage Guide
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