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Asia-Pacific's Growing Role in Global Clinical Trials

Published by: CenterWatch

Published: Mar. 1, 2008 - 168 Pages


Table of Contents



EXECUTIVE SUMMARY

INTRODUCTION

CHAPTER ONE

Regulatory Process Changes Could Speed Growth

CHAPTER TWO

China Speeds Up Regulatory Time lines

CHAPTER THREE

India’s Evolving Regulatory Process

CHAPTER FOUR

Will Australia’s and New Zealand’s Regulatory Agencies Merge?

CHAPTER FIVE

South Korea’s Acceptance of INDs Propels Growth

CHAPTER SIX

Japan Eager to Participate in Asia-Pacific’s Success

CHAPTER SEVEN

Hot Talent Market

CHAPTER EIGHT

EDC Adoption

CHAPTER NINE

The Next Hot Spot: Vietnam

CHAPTER TEN

Future Outlook

CHAPTER ELEVEN

The Next Phase: Astra Zeneca Leads the Way

CHAPTER TWELVE

CenterWatch Survey Results, Other Charts and Data

CHAPTER THIRTEEN

Clinical Research News Highlights Across

Asia-Pacific in 2007

CHAPTER FOURTEEN

Company Profiles

CHAPTER FIFTEEN

Drug Development Pipeline in Asia-Pacific

APPENDIX A

A New Era Begins for India’s Clinical Research Market

APPENDIX B

China on Fast Track to Becoming Developed Market

APPENDIX C

Top 20 Pharma Flock to China ,SetUp CRUs

APPENDIX D

Select List of CROs in Asia-Pacific

ABOUT CENTERWATCH

Abstract

Global clinical trials initiated in the Asia-Pacific region increased 50% between 2005 and 2006, a dramatic one year spurt of growth led by Taiwan, Korea and India. But this will not be an isolated incident. Countries in the region have continued to make changes for the better in their respective clinical research environments to allow for even more growth. With strong economic drivers, more than one-third the earth’s population and inherent challenges being addressed by an increasingly savvy industry, there is no end in sight for the Asia- Pacific region’s growth in clinical research.

Although the Asia-Pacific region comprises countries that are markedly different from each other, those countries share important commonalities that attract big pharma and biotech to the region to conduct clinical research. Drivers include the requirements for greater numbers of patients for clinical trials that have become increasingly complex, faster patient enrollment times and the fact that some countries are emerging as large economic powers. In addition, because investigative sites in Asia Pacific have significantly fewer enrollment delays of one month or more compared with the U.S., according to the CenterWatch 2006 survey of investigative sites in Asia-Pacific, the cost savings to be gained from conducting clinical research in the region are substantial.

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