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Reportlinker Adds Orphan Drugs in Asia: Guidelines and Regulatory Requirements to Help Orphan Drug Products Enter the Asian Market 2011
Date:4/27/2011

This report is 109 pages.

TABLE OF CONTENTS

I. Introduction 

A. Global Outlook on rare diseases

B. Development of Orphan Drug Legislation

C. Well-Known Rare Diseases

D. US FDA Contact Information

E. US Orphan Drug Associations

F. US FDA Orphan Drug Approvals

II. Overview of Asia 

A. The Asian Economy

B. The Pharmaceutical Markets in Asia

III. Orphan Drugs in Asia 

A. Do orphan drugs have potential in Asia?

B. Why seek orphan drug status?

IV. Issues to Consider Prior to Orphan Drug Registration 

A. Introduction

B. Are treatment options already available in the country?

C. Is your drug superior to those already on the market?

D. Conclusion

V. Japan 

A. Introduction

B. Ministry of Health, Labor and Welfare

C. Pharmaceuticals and Medical Devices Agency

D. Orphan Drugs in Japan

E. Health Authority Contact Information

F. Orphan Drug Associations

G. Orphan Drugs Approved in Japan

H. Orphan Drugs Designated in Japan

VI. Taiwan 

A. Overview

B. Taiwanese Health Authorities

C. Health Insurance Scheme

D. Orphan Drugs in Taiwan

E. Health Authority Contact Information

F. Orphan Drug Associations

VII. Korea 

A. Overview

B. Drug Registration Overview

C. Orphan Drugs in Korea

D. Health Authority Contact Information

E. Orphan Drug Associations

F. Orphan Drugs Approved in Korea

VIII. Hong Kong 

A. Overview

B. Hong Kong Health Authority

C. Orphan Drugs In Hong Kong

D. Health Authority Contact Information

IX. China 

A. Overview

B. Pharmaceutical Market

C. China Health Authority

D. Drug Registration Process

E. Drug Pricing

F. Orphan Drugs in China

G.
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