Back to On-demand Webcast: CFDA Registration Requirement for Imported Class II/III Medical Devices
1.00 RAC

On-demand Webcast: CFDA Registration Requirement for Imported Class II/III Medical Devices

An on-demand recording of the RAPS Webcast, CFDA Registration Requirements for Imported Class II/III Medical Devices, originally recorded on December 2015.


Credits:
1.00 RAC

  • List Price: $300.00
  • Member Price: $200.00

 
Want to save more?
to see if you qualify for a lower rate.
Members: save $100.00 or more
Item Details:

With the implementation of Provisions for Medical Device Registration on 31 October 2014, there were lots of changes for CFDA registration requirements related to medical devices, especially with treating domestic and imported medical devices equally. The newly added request compared to the...

Back to On-demand Webcast: CFDA Registration Requirement for Imported Class II/III Medical Devices
View More

» View the Table of Contents

Fundamentals of US Regulatory Affairs, Eighth Edition

Table of Contents

Section I: General Information
Chapter 1 FDA and Related Regulatory Agencies
Chapter 2 History of Food, Drug and Cosmetic Law
Chapter 3 Overview of Drug, Biologic and Device Regulatory Pathways
Chapter 4 FDA Communications and Meetings
Chapter 5 Preparing for Key FDA Meetings and Advisory Committee Meetings
Chapter 6 Crisis Management
Chapter 7 Health Technology Assessment
Chapter 8 Good Laboratory Practice Regulations
Chapter 9 Clinical Trials: GCPs, Regulations and Compliance
Chapter 10 Current Good Manufacturing Practice and Quality System Design