上市后临床跟踪管理程序.docVIP

上市后临床跟踪控制程序 文件编号： QP-29 版本：A/0 生效日期： 页码： NUMPAGES 3 编制： 审核： 批准： Purpose The purpose of this work instruction is to define the process to determine and document whether a post-market clinical follow-up study is required forTDI Foot/Ankle Array 8ch medical devices bearing the CE mark. The process w