醫(yī)療器械操作規(guī)程

1、XXXXXX有限公司醫(yī)療器械經(jīng)營質(zhì)量管理體系文件醫(yī)療器械操作規(guī)程目錄醫(yī)療器械操作規(guī)程目錄1.文件管理操作規(guī)程...................................................................................................12.采購操作規(guī)程..........................................................

2、.................................................33.驗(yàn)收操作規(guī)程...........................................................................................................54.儲(chǔ)存保管操作規(guī)程............................................

3、.......................................................65.養(yǎng)護(hù)操作規(guī)程...........................................................................................................76.出庫復(fù)核操作規(guī)程......................................

4、.............................................................97.銷售操作規(guī)程.........................................................................................................108.不合格醫(yī)療器械確認(rèn)及處理操作規(guī)程.........................

5、........................................129.售后服務(wù)操作規(guī)程.................................................................................................1510.售后退回操作規(guī)程..........................................................

6、.....................................1711.診斷試劑購進(jìn)操作規(guī)程.......................................................................................1812.診斷試劑驗(yàn)收操作規(guī)程..................................................................

7、.....................2013.診斷試劑儲(chǔ)存與出庫操作規(guī)程...........................................................................2114.診斷試劑銷售與售后服務(wù)操作規(guī)程...................................................................2315.診斷試劑運(yùn)輸操作規(guī)程....

8、...................................................................................2516.診斷試劑銷后退回操作規(guī)程...............................................................................2617.不合格診斷試劑的確認(rèn)及處理操作規(guī)程...................

9、........................................27XXXXXX有限公司醫(yī)療器械經(jīng)營質(zhì)量管理體系文件25.6.質(zhì)量管理體系文件的回收：作廢的文件，綜合辦公室應(yīng)進(jìn)行登記并回收，防止作廢的文件繼續(xù)留在工作現(xiàn)場。5.7.質(zhì)量管理體系文件的執(zhí)行監(jiān)督與檢查：每年質(zhì)量管理部通過日常的管理和組織質(zhì)量體系內(nèi)審的形式檢查質(zhì)量管理體系文件的落實(shí)情況，對(duì)存在的問題提出糾正和預(yù)防措施。5.8.行政類文件的編制：綜合辦公室根據(jù)公司