European Federation of Pharmaceutical Industries / World Health Organization / ICH Secretariat / U.S. Food and Drug Administration / European Commission / WHO Collaborating Centre for International Drug Monitoring / European Union / Center for Drug Evaluation and Research / ICH Steering Committee / Ministry of Health / Japan Pharmaceutical Manufacturers Association / Council for International Organizations of Medical Sciences / International Federation of Pharmaceutical Manufacturers Associations / ICH M2 Expert Working Group Members Name Organization / /
Person
Bowen PhRMA / Yuichi Nagoshi Hitoshi Asano Tadao / Mihoko Okada Shigekoto Kaihara Daisuke / Hitoshi Asano Tadao Akiyama Harv / Robert Kapitany / Mervyn Mitchard Gabriele Disselhoff Marc / Daisuke Koide Kenichi Tamiya / Esteban G. Juarros Antonia Rana / R. Chapman Robin Jones George / Keiji Sawamukai Yuichi Nagoshi Hitoshi / Melissa R. Chapman / Robert Hizer Rick Bowen / George P. George / Gabriele Disselhoff Marc Elbet / /
Position
Director for Technology Policy / /
Product
Specifications ICH ICSR DTD Version 2.1 / Step 3 version 5 / Step 3 5 / Specifications ICH ICSR DTD 2.1 / /
ProvinceOrState
Maryland / /
Technology
SGML processor / SGML / Information Technology / DTD / document technology / DOCUMENT TYPE DEFINITION / /
Electronic Transmission of Individual Case Safety Reports Message Specification Document Version 2.3 November 9, 2000 INTERNATIONAL CONFERENCE ON HARMONISATION OF TECHNICAL REQUIREMENTS FOR REGISTRATION OF PHARMACEUTICAL