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Session Chair(s)
Lembit Rago, DrMed, MD, PHD
Secretary General
Council for International Organizations of Medical Sciences (CIOMS), Switzerland
Learning Objective : Getting arguments to answer the question if and how technology can be utilized as helpful tool facilitating the sharing of workload in Drug Regulatory Affairs. Understand the prerequisites how interoperability can be supported between multiple systems to be developed in the pharmaceutical regulated environment
Speaker(s)
Why is Regulatory System Strengthening Important?
Lembit Rago, DrMed, MD, PHD
Council for International Organizations of Medical Sciences (CIOMS), Switzerland
Secretary General
Telematics Goes Global – How Can Technology Strengthen Regulatory Systems?
Klaus Menges, DrMed
BfArM, Germany
Project Manager
The International Coalition of Medicines Regulatory Authorities (ICMRA) Role in Capacity Building: Where Are the Gaps and Overlaps?
Toshiyoshi Tominaga, PHD
SunFlare Co., Ltd, Japan
Life Science Department, Advisor
Regulating Medical Devices: Bridging Gaps on a Global Scale
Josee Hansen
World Health Organization, Switzerland
Senior Advisor