Back to New China Medical Device Regulations: Best Practices for Clinical Trials (On-demand Webcast)

New China Medical Device Regulations: Best Practices for Clinical Trials (On-demand Webcast)

An on-demand recording of the RAPS Webcast, New China Medical Device Regulations: Best Practices for Clinical Trials recorded on 18 February 2015.

  • List Price: $395.00
  • Member Price: $295.00

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

China’s new medical device regulations went into effect 1 October 2014. This session will review the impact of the new regulations to date and focus specifically on challenges around clinical trials in China and new guidance’s issued about the execution of clinical trials and opportunities to avoid...

Back to New China Medical Device Regulations: Best Practices for Clinical Trials (On-demand Webcast)
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