Tri-Conference 2008
会议概要 展销前置会 地点 参展/赞助 大会议程 询问 报名
会议将同时进行
Fluidigm
Thermo
Aviva Systems Biology
Biobase
Caprion Proteomics
Expression Analysis
Ingenuity
Scientia Advisors
Theranostics Health
Tripos
Wafer GEN
CROWNBIO
Leomics Associates
PCO
BioCentury
Bio IT World
SCIENCE AAAS
TheScienteist




Clinical Trials Asia 概要

[  概要   |   展销前置会   |   1日目   |   2日目   |   3日目   |   Catalog(PDF)  ]


第2回 亚洲治疗实验 - 印度、中国、东南亚中治疗实验的企画、设定、实施战略
2008年3月26~28日

  1. 印度、中国、东南亚中治疗实验设计和企画
  2. 伦理审查委员会过程的管理
  3. 印度的安全性报告和医药品安全对策实施
  4. 亚洲的规定动向介绍
  5. 亚洲的治疗实验的设计及实施上的战略及战术检讨事项:从其它事例得到的教训
  6. 物流问题的克服和合作者(partner)的管理,规范(compliance)的保证

FEATURED PRESENTATIONS:

Utilizing and Integrating Data from China to Mutually
Support Global and Local Applications

James Cai, M.D., Vice President, R&D and Business
Development, AstraZeneca Pharmaceuticals, China

Country and Site Selection for Global Clinical Trials
Fidela Ll. Moreno, M.D., Executive Director, Global Development
Operations, Asia and Latin America, Amgen Inc.

Recent Regulatory Changes in India
Chandrashekhar Potkar, M.D., Director, Clinical Research,
Pfi zer Ltd. (India)

Optimizing Return on Investment (ROI) of Multinational
and Domestic Clinical Trials in China

Min Irwin, M.D., Ph.D., Medical Director of BSP China, Bayer
HealthCare Company Ltd.

Roles and Functioning of Institutional and Independent
Ethics Committees in India

Y.K. Gupta, Head, Dept. of Pharmacology; Coordinator, Zonal
Pharmacovigilance Centre, All India Institute of Medical Sciences

Safety Reporting in India Clinical Research Environment
Kamala Rai, M.D., Research Director, MSD Pharmaceuticals Pvt
Ltd; Medical Director, Merck (India)

Accelerate Oncology Clinical Development in Asia
Michael Shi, Director and Biomarker Project Leader, Exploratory
Oncology Development, Novartis Oncology

Are You Ready for an FDA Inspection?
Cherif Benattia, M.D., Vice President, Pharmacovigilance &
Public Health, Vertex Pharmaceuticals

The Strategic Planning Behind the Clinical Site Allocation
in Emerging Economies: An Industry-Wide View

Fabio Thiers, M.D., M.Sc., Ph.D., Research Associate, MIT Center
for Biomedical Innovation, MIT

SESSIONS:

  • Designing and Planning Trials in India, China and Southeast Asia

  • Managing the Ethical Review Committee Process

  • Safety Reporting and Implementation of Pharmacovigilance Practices at Indian Sites

  • Effectively Identifying, Selecting and Engaging Clinical Sites

  • Navigating the Regulatory Landscape throughout Asia

  • Strategic and Tactical Considerations when Designing and Conducting Trials in Asia: Learning from Others

  • Overcoming Logistics, Managing Partners and Ensuring Compliance

INTERACTIVE PANELS:

  • Utilizing and Integrating Local Clinical Data from Asia to Mutually Support Global and Regional Applications

  • Effectively Identifying, Selecting and Engaging Clinical Sites

  • Navigating the Regulatory Landscape throughout Asia

  • Realistic Opportunities and Main Challenges to Conducting Trials in India, China and Southeast Asia

Catalog(PDF) Download
Schedule

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