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Speakers

Understand Impending Changes for Harmonised Submission and Assessment Requirements

March 6-7, 2018
  • Brussels, Belgium

Behtash Bahador
Senior Manager, Quality and Compliance, Communicating Trial Results
Center for Information & Study on Clinical Research Participation (CISCRP)

Matt Cooper
Business Development & Marketing Director
NIHR Clinical Research Network Coordinating Centre

Moira Daniels
Vice President, Head of Regulatory Affairs
UCB

Sini Eskola
Director Regulatory Affairs
European Federation of Pharmaceutical Industries and Associations (EFPIA)

Marie Manley, LLM
Partner and Head of the Regulatory Practice
Bristows LLP, United Kingdom

Greet Musch, Ph.D.
General Director Pre-Marketing Authorisation
Federal Agency for Medicines and Health Products (FAMHP), Belgium

Anastassia Negrouk
Head of International Regulatory and Intergroup Unit
European Organization for Research and Treatment of Cancer (EORTC)

Christopher Price
Manager Global Regulatory Affairs Oncology
Merck KGaA

Tania Snioch
Director of Healthcare
GS1

Josefine Sommer
Associate
Sidley Austin LLP

Richard Stephens
Consumer Lead, Chair of Consumer Forum
National Cancer Research Institute (NCRI)

Cristiana Spontoni
Partner
Jones Day

Matthias Zerm, Ph.D.
Global Clinical Development
Lead Expert Clinical Trial Disclosure and R&D Processes
Merz Pharmaceuticals GmbH

Behtash Bahador
Senior Manager, Quality and Compliance, Communicating Trial Results
Center for Information & Study on Clinical Research Participation (CISCRP)

Matt Cooper
Business Development & Marketing Director
NIHR Clinical Research Network Coordinating Centre

Moira Daniels
Vice President, Head of Regulatory Affairs
UCB

Sini Eskola
Director Regulatory Affairs
European Federation of Pharmaceutical Industries and Associations (EFPIA)

Marie Manley, LLM
Partner and Head of the Regulatory Practice
Bristows LLP, United Kingdom

Greet Musch, Ph.D.
General Director Pre-Marketing Authorisation
Federal Agency for Medicines and Health Products (FAMHP), Belgium

Anastassia Negrouk
Head of International Regulatory and Intergroup Unit
European Organization for Research and Treatment of Cancer (EORTC)

Christopher Price
Manager Global Regulatory Affairs Oncology
Merck KGaA

Tania Snioch
Director of Healthcare
GS1

Josefine Sommer
Associate
Sidley Austin LLP

Richard Stephens
Consumer Lead, Chair of Consumer Forum
National Cancer Research Institute (NCRI)

Cristiana Spontoni
Partner
Jones Day

Matthias Zerm, Ph.D.
Global Clinical Development
Lead Expert Clinical Trial Disclosure and R&D Processes
Merz Pharmaceuticals GmbH