Efficiently manage, develop and create a compliant TMF structure for PMDA and global inspections.
For the last six years, ExL's Trial Master File Series has explored the challenges and evolution of the TMF landscape in the United States and United Kingdom - but we know the obstacles you and your colleagues face greatly vary depending on where you release your product. We have created the Asia-Pac Trial Master File Summit to address this area's need for an event with a regional focus, and to share how to efficiently manage, develop and create a compliant TMF structure that meets both PMDA and global requirements.
Website: https://go.evvnt.com/64700-0
Date and Time: On Monday October 03, 2016 at 8:00 am ends Tuesday October 04, 2016 at 5:00 pm
Venue details: The Westin Tokyo, 1-4-1 Mita Meguro-ku, Tokyo, 153-8580, Japan
Price:
Conference - Register by 2016 August 19: JPY 180000,
Conference - Register by 2016 September 30: JPY 200000,
Conference - On-site Registration: JPY 220000
Speakers: Saki Akihara, Amer Alghabban, Yong Guo, Yoshiko Hara, Vinita Leslie, Yasuhiro Marukawa, Kiyoko Matsushima, Lisa Mulcahy, Karen Roy, Kazunori Takeda, Jamie Toth, Tatsushi Tsuda, Keiko Watanabe, Karyopharm Therapeutics, Hansoh Pharmaceutical Group, Daiichi Sankyo Japan, Biogen, Eisai, Pfizer Japan, Mulcahy Consulting, Phlexglobal, Sumitomo Dainippon Pharma
