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14

25 – 28 March 20
g
The Westin Beijin
Chaoyang, China

East Asia
provals in China &
ug & Clinical Trial Ap
Accelerating Dr

What’s New in 2014?
Key Regulatory Update from the National
Institute for Food & Drug Control, China

Pediatric Investigational Plans (PIPs)

MORE Drug Regulations & Case Studies

Interactive & Open Discussion Session on
Quality by Design (QbD)

Electronic Regulatory Affairs
Learn from China Industry Best Practices

Discover Bridging Studies and Waiver
Opportunities

Pharmaceutical Marketing Regulations

Drug-Device Combination Products

2014 Regulatory Experts Include:

Prof. Ning Bao Ming

Annette Chiu

Stewart Geary

Deputy Director, Division of
Chemical Drugs/GMP
Inspector, National
Institute for Food and
Drug Control, Agency of
the CFDA, China

Regulatory & Medical Affairs
Director, GlaxoSmithKline,
Chairperson of the Regulatory
Affairs Committee,
Hong Kong Association
of the Pharmaceutical
Industry, Hong Kong

Vice President/Deputy Director, President,
Corporate Regulatory
BravoBio, China
Compliance & QA, Eisai Japan,
Director, The Japanese
Association of
Pharmaceutical Medication
(JAPhMed), Japan

Dr Wu Ke

May Wei
Global Regulatory Strategist,
Bayer Healthcare, China

PLUS! Informative Workshops on:
PRE-CONFERENCE WORKSHOPS • 25 MARCH 2014

POST-CONFERENCE WORKSHOPS • 28 MARCH 2014

A Preparing and Submitting Dossiers for Generic Drug Approval
B Gaining Global Approvals of Biosimilars

C Regulatory Strategies for Emerging Market Access
D Pediatric Drug Development

www.pharmaregulatoryasia.com
Produced by:

Supporting Organisation:

Media Partners:

Life
Sciences

International Marketing Partner:

REGISTER NOW! Customer Service Hotline: +65 6508 2401 / +86 21 2326 3680

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