WeChat
Sina Weibo
QQ
Baidu Tieba
English
English
|
中文
Home
Home
About us
Nav
Medical Device
Nav
SMO
Nav
Cosmetics
Nav
FSMP
Nav
Maris Regulations Class
Nav
Company profile
Group news
Founder introduction
Cooperative customers
Job Opportunities
Contact us
Class I medical devices
Class II medical devices
Class III medical devices
Special medical devices
Medical device registration
Clinical trial
Clinical evaluation
Classification and definition
Subsidy support
Detection agent
Product System Setup
Registrant system
Domestic responsible person
Regulatory dynamics
SMO service
Company Branch
Project experience
Vocational training
Registration and filing of cosmetics
Cosmetics testing agent
Cosmetics customization
Cosmetic trademark registration
Cosmetics domestic agent
Cosmetics sales support
Vocational training & qualification examination
Plant Set-up
Clearance
Cosmetics approval transfer
Listing risk assessment
Professional regulations consultation
Warehouse management
Trends in cosmetics regulations
Full nutrition special medical food
Non nutritional special medical food
Specific full nutrition special medical food
Detection agent
Data preparation and review
Expert training
System service
Regulatory dynamics
News Detail
流程 | 医疗器械临床稽查内容及流程
Issuing time:2020-08-12 14:20
医疗器械临床研究机构及人员资质审核
医疗器械临床试验方案评估
临床项目现场稽查、研究中心稽查
临床研究基本文件稽查
医疗器械注册临床评价资料稽查
医疗器械临床稽查报告编制
CAPA计划提出及执行
Maris Group
010-67166800
联系邮箱：bd@maris-reg.com
cosmetics@maris-reg.com
fmsp@maris-reg.com
联系电话 : 400-853-5405
医疗器械咨询：+86-10-67166800
化妆品注册咨询：+86-10-67168320
特医、保健食品注册咨询：
87-87-
8671
+13021067716
联系地址：
北京市东城区广渠门内大街新裕商务大厦A座9层
Login
Login
Register for free>
Login by：
◆
My Profile
◆
leave a message
◆
View Mobile Site
◆
back to the top
◆
