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Session Chair(s)
Maia Uuskula
Head of the Bureau of Pharmacovigilance
State Agency of Medicines, Estonia
Speaker(s)
New Approaches to Benefit/Risk Management Planning in the EU
Sabine Straus, MD, PHD, MSC
Medicines Evaluation Board (MEB), Netherlands
Former PRAC Chair
Innovative Industry Experience Since 2012 and Reflections on New EU Guidance
Valerie E. Simmons, MD, FFPM
Eli Lilly and Company Ltd, United Kingdom
Senior Medical Fellow, Global Patient Safety
Generics Industry Experience since 2012 and Reflections on New EU Guidance
Katarina Nedog, MSC
EFPIA - European Federation of Pharmaceutical Industries and Associations, Belgium
Associate Director
Panel discussion
June Raine, MD, MSC, FRCP
Medicines and Healthcare Products Regulatory Agency (MHRA), United Kingdom
Chief Executive
Panel Discussion
Peter Bachmann
Federal Institute for Drugs and Medical Devices (BfArM), Germany
Retired from Head International Liaison Office and Conferences, Executive Depart