ICH Project The 25th ICH Public Meeting

December 05, 2011

The 25th ICH Public Meeting was held in Japan which took place at the Nissho Hall, Minato-ku in Tokyo on December 05, 2011.This Public Meeting aimed to provide an opportunity to give the public updated information on the progress made during the ICH Meeting in Seville in November, 2011, and on the status of the various ICH Guidelines under development with a follow-up Q & A session.

The public meeting was jointly organized by the Japan Pharmaceutical Manufacturers Association (JPMA) and the Pharmaceutical and Medical Device Regulatory Science Society of Japan (PMRJ, non-profit organization), and supported by the Federation of Pharmaceutical Manufacturers' Associations of Japan, the Pharmaceutical Manufacturers' Association of Tokyo, Osaka Pharmaceutical Manufacturers Association and Japan Pharmaceutical Association.

Working Language
Japanese
Simultaneous English-Japanese Translation
Not Available
Location
Nissho Hall, 2-9-16, Toranomon, Minato-ku Tokyo, Japan
Date
December 5, 2011 10:00 a.m. -4:00 p.m.

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  Presentation materials Speakers

 

01_Welcoming Address

Kohei Wada, JPMA

02_ Overview of ICH Topic

Yasuko Inokuma, MHLW

Safety Topics

03_ S1A: Need for Carcinogenicity Studies of Pharmaceuticals

Akiyoshi Nishikawa, MHLW(NIHS)

04_ M7: Assessment and Control of DNA Reactive(Mutagenic) Impurities in Pharmaceuticals to Limit Potential Carcinogenic Risk

Shigeki Sawada, JPMA

Topics for the Electronic Exchange of Information

05_ M5: Data Elements and Standards for Drug Dictionaries

Maiko Suzuki, MHLW(PMDA)

Efficacy Topic

06_ E3: Structure and Contents of Clinical Study Reports

Kayo Shinohara, MHLW(PMDA)

07_E2C(R2): Clinical Safety Data Management; Periodic Benefit-Risk Evaluation Report (PBRER)

Yukiko Watabe, JPMA

Quality Topics

08_ Q3D: Guideline for Metal Impurities

Chikako Yomota, JPMA

09_Q11:Development and Manufacture of Drug Substances(Chemical Entities and Biotechnological/Biological Entities)

Kiyotoshi Matsumura, JPMA

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