Welcome to Keren Pharmaceutical Technology Consulting Co,.Ltd.!
Home Contact us Chinese View
 

QQ

QQ

QQ


Wechat

400-806-2855

在线客服
Home >> Medical device registration >> China CFDA registration for importing medical devices
 
Clinical evaluation
Medical writing
Clinical trials management
Clinical trials monitoring
QA
Data management
Statistical report
Medical device registration
China CFDA registration for importing medical devices
China CFDA registration for domestic medical devices
Manufacturing license in China
GMP Setup
China CFDA registration for importing medical devices

1.  License application of medical device II, III

2.  Registration of imported medical device

3.  licensing agent for medical device management

4.  consulting for GMP (Good Manufacturing Practice) of medical device

5.  Providing guidance on quality-managing system for medical device enterprise.

6.  Registration agent for IVD II, III

7.  Inspection service on medical device or related fields.

Clinical evaluation
Medical writing
Clinical trials management
Clinical trials monitoring
QA
Data management
Statistical report
Medical device registration
China CFDA registration for importing medical devices
China CFDA registration for domestic medical devices
Manufacturing license in China
GMP Setup
Contact us
Address: room 1406, building 2, No. 66 street, Jianggan District, Hangzhou
Tel:0571-87555135 0571-87551779
Fax:0571-87555135
Email:xiang.junqing@cro.org.cn
 
 
Hangzhou Keren Pharmaceutical Technology Consulting Co,.Ltd. 浙ICP备14019432号