Chinese
English
HOME
ABOUT US
SERVICE
NEWSLETTER
DOWNLOAD
CONTACT US
・VIACERT INTRODUCTION
・Our Team
・Client Testimonial
・CFDA Medical Device Registration
・Medical Device Company
・GMP & ISO13485 SYSTEM
・Clinical Trial of Medical Device
・Testing of Medical Device
・Company News
・Policy laws & regulations
・Download Files
・Contact
・Enquire Form
Viacert
Professional service
One-stop-shop service providing global entry solution
High-Speed registration and regulatory compliance
Efficent and low cost
Email:
info@via-cert.com
Tel:
+86 15301675515
HOME
→
SERVICE
CFDA Medical Device Registration
Registration of Class I Import Medical Device
Registration of Class II Import Medical Device
Registration of Class III Import Medical Device
Medical Device Restriction
Medical Device Manufacture License
Medical Device Trading License
Act as China Agency office
Act as After-sale Service Agency in China
GMP & ISO13485 SYSTEM
China Medical Device GMP Consulting
Implantable Medical Device GMP
Sterile Medical Device GMP
ISO 13485 Certification Consulting
Testing of Medical Device
Clinical Protocols
Clinical Trial Schema
Medical Statistics
Clinical Trial Report
Clinical Trial of Medical Device
CFDA Regulatory Affairs
Product Registration Standards
Follow Up Whole Testing Procedures
Implantable Medical Device GMP
The implement rule and assessment standard for QMS of implantable medical device. (download)
COPYRIGHT © Shanghai Viacert. All rights reserved 沪 ICP 备11015076
