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Conference to Address How to Improve the Value and Quality of New Drugs in East Asia

Tokyo, Japan — Mar 31, 2014

Professionals from across East Asia will discuss the latest hot topics in all stages of drug development at the 8th DIA Annual Conference in Japan for Asian New Drug Development.

The event will return for its eighth year on May 22 to 23, at Sola City Hall, Ochanomizu in Tokyo. Expert speakers will share information and experiences regarding the current situation of new drug development in the emerging East Asia region, and provide advice on how to improve the value and quality of new drugs.

Sessions will focus on the latest regulatory information, early phase clinical trial, collaboration between academic organizations, regulatory inspection, regional study communications and late phase development strategy.

The conference will feature presentations on the latest regulatory trends and regional clinical trials in Asia from industry leaders and high-profile representatives from Asian regulatory authorities, including the Pharmaceuticals and Medical Devices Agency (PMDA), China Food and Drug Administration (CFDA), and the Ministry of Food and Drug Safety in Republic of Korea. Academic speakers from Japan, China and Korea will also provide their future visions of new drug development and the role of academia collaboration in East Asia.

Program chair Hidetoshi Shuto, Corporate Executive for Astellas Pharma Inc.,said: “Drug development in East Asia has become extremely vigorous as the interests of organizations related to drug development expand. Such organizations are now not only interested in the advancement of drug development, but also the maximization of generated value and the improvement of quality in new drug development.

“In order to facilitate drug development under the revised regulations for optimal regulatory circumstances, professionals involved in drug development face various challenges. Furthermore, collaboration to work towards drug development beyond each country’s boundaries is strongly desired in this era of globalization. This conference will discuss these topics and much more.”

Other session highlights include:

  • Early Phase and Regional Clinical Trials in Asia/Academia Collaboration in East Asia
  • East Asian Regulatory Update on Global Clinical Trials
  • Trend of GCP Inspection
  • Optimal Development Strategies Based on Differences in Culture and Health Care Setting
  • Effective and Efficient Communication in Asia Regional Studies
  • Panel Discussions
For more information about the event, or to register, visit www.diahome.org/Japan-8thNewDrugDev

 


Contact: Keiko Cambridge

Event Planning Manager
+81.3.5575.2130
Keiko.Cambridge@diajapan.org

 

 

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ABOUT DIA: DIA is the global connector in the life sciences product development process. Our association of more than 18,000 members builds productive relationships by bringing together regulators, innovators and influencers to exchange knowledge and collaborate in an impartial setting. DIA’s network creates unparalleled opportunities for the exchange of knowledge and has the interdisciplinary experience to prepare for future developments. The dedicated efforts of DIA staff, members and speakers enable DIA to provide a comprehensive catalogue of conferences, workshops, training courses, scientific publications and educational materials. DIA is a global community representing thousands of stakeholders working together to bring safe and effective products to patients. DIA is an independent, nonprofit organization with its global center in Washington, D.C., USA; regional offices covering North and South America (Horsham, Penn., USA); Europe, North Africa and the Middle East (Basel, Switzerland); and Japan (Tokyo), India (Mumbai) and China (Beijing). For more information, visit www.diahome.org.