成·人午夜在线观看_日本一点不卡高清_午夜剧场a级毛片_国产精品免费AV片在线观看

Medical Device Regulations, Registration, System and Clinical One-stop Service
24x7 service hotline:+86-0571-86198618 Simplified Chinese English
Current location: Default>Services>Contract Research Organization
醫(yī)療器械臨床服務流程
CREATE TIME:2018-06-29 11:32BROWSE TIMES:2014
根據(jù)《醫(yī)療器械監(jiān)督管理條例》(國務院令第650號)的規(guī)定,第Ⅰ類醫(yī)療器械實行產(chǎn)品備案管理,不需要進行臨床試驗,但需要提交臨床評價資料;第Ⅱ、Ⅲ類醫(yī)療器械注冊時,應當進行臨床試驗(免于進行臨床試驗的第Ⅱ類醫(yī)療器械目錄;免于進行臨床試驗的第Ⅲ類醫(yī)療器械目錄的醫(yī)療器械除外);免于進行臨床試驗的醫(yī)療器械,在進行注冊申報時,仍需提供臨床評價資料。
PREVIOUS: IVD clinical trial workflow chart
NEXT: NOTHING

Friend link:

Copyright © 2018 Hangzhou Zhengbiaoke Enterprise Management Co., Ltd. CHINA ICP NO.18025678 Technical support:XIHEKEJI.COM