Driving value in phase IIIb & IV trials

Late Phase Drug Development World 2011 - Speaker list

The Customer Show is the only CRM event in the Middle East
 

Dr Enrica Alteri

Head Medical Safety Group, Global Drug Safety Neurodegenerative Autoimmune Inflammatory Diseases

Merck Serono

Dr. Enrica Alteri received her Medical Doctorate from the University La Sapienza in Rome, Italy. She completed a post-doctoral Fellowship in the Department of Immunopathology of the National Cancer Institute (USA). A Diploma in Pharmaceutical Medicine completed...

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Gary Appio

Head - US Safety Risk Management

Novartis

Andrew Bate

Senior Director, Analytics Team Lead

Pfizer Inc

Andrew is Senior Director, Analytics Team Lead in Epidemiology at Pfizer Inc. This position oversees the provision of methodological and analytic expertise to the Epidemiology group in support of drug development and safety evaluation activities worldwide. Prior to...

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Neil Brickel

Safety Development Leader

GSK

Neil qualified from the London Hospital Medical College (University of London) in 1991 and gained Membership of the Royal College of Physicians in 1994. In October 2000, Neil entered the Pharmaceutical industry, initially in Medical Affairs roles in UCB Pharma UK...

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Cara Cassino

Vice President, Medicines Development Group

Pfizer

Dr. Cassino is Vice President of the Medicines Development Group for Pulmonary Vascular Disease (PVD) and Rare Diseases at Pfizer Inc. in NY. In this capacity, she leads a global team responsible for worldwide clinical development and medical affairs...

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Patrick Chassaigne

Director, Late Phase Solutions

Medidata

Day Two- Thursday 8th December 2011, 12.30pm

Leveraging enabling technologies to conduct observational research

Andrea Chioato

Executive Director, Head Profiling Autoimmunity, NIBR - Translational Medicine

Novartis

Day Two- Thursday 8th December 2011, 9.50am

Autoinflammatory diseases: trial design challenges

Philippe Close

Chief Safety Officer and EU/EEA QPPV

Novartis Pharma AG

Day Two- Thursday 8th December 2011, 11.15am

Signal detection in pharmacovigilance

Scott Dixon

Head of Product Strategy for Late Phase and Direct to Patient Solutions

Oracle Health Sciences

As Global Product Strategist for Late Phase and ePRO, Scott Dixon focuses on product development and the operational aspects of late phase research and ePRO. Mr. Dixon was in a similar capacity at Phase Forward prior to its acquisition by Oracle. Previous to...

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Day Two- Thursday 8th December 2011, 1pm

Keeping patients at the core of post marketing studies

Dr Aidan Gill

Medical Director UK & Ireland, Human Genetic Therapies Business Unit

Shire

Day Two- Thursday 8th December 2011, 9.25am

Real World data, Real World Outcomes in Rare Diseases

Maria C. Harrison

Vice President of Late Phase Services

PRA International

Day One- Wednesday 7th December 2011, 2pm

Opening remarks from the chair

Elizabeth Hernberg-Stahl

Senior Consultant

Late Phase Solutions Europe AB

Elizabeth Hernberg-Ståhl has almost 20 years of international experience from Pharmaceutical Industry in developing and managing global patient registries on rare orphan diseases. She has during these years gained an in-depth expertise in designing and managing...

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Pre-conference workshop, 9am

Overview:

Magnus Jaderberg

Chief Medical Officer, Europe

BMS

Pharmaceutical physician with over 20 years in various R/D functions including clinical research, medical affairs, pharmacovigilance, strategic product development and general management. Lecturer in drug development at King’s College, London.

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Yue Kang

Head of Clinical Development

Abbott

Yue KANG, M.D., M.Sc, Affiliate Medical Director, Abbott Laboratories China, since 2008. Responsible for the medical department performance, including clinical research (ph 1~4); medical affairs; drug safety, medical information, medical operation, and...

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Day Two- Thursday 8th December 2011, 2.30pm

Late phase drug development in China

Michael Meyers

Compound Development Team Leader

J&J

Liz Mitchell

VP Medicine Development Leader, Neurosciences MDC

GSK

• >20 years direct experience in pharmaceutical development, specialising in neurosciences and late stage drug development • Career has evolved through neuropharmacology research scientist, to clinical development, project management and leadership of pharmaceutical...

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Ebrahim Naderali

Medical Affairs(Endocrinology,Biological Medicines),Prof of Metabolic,Diabetes,Obesity&Cognative Research-Liverpool Hope University

Pfizer

Krista A Payne

Senior Director & Senior Research Scientist

UBC

Paul Reilly

Director, Cardiovascular Medicine

Boehringer Ingelheim Pharmaceuticals

Paul Reilly has been active in clinical research in the pharmaceutical industry for over 30 years, most of the time with Boehringer Ingelheim. He has been active in both corporate and operational roles in Canada, Europe and the United States. He has planned and...

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Agnes Rivaille

Scientific Affairs, Director, Late Phase Services

PRA International

Day One- Wednesday 7th December 2011, 4.10pm

Data Quality and NIS: Definition and operational considerations

Jani Söderhäll

Founder

PCPal

Pre-conference workshop, 9am

Overview:

Declan Tobin

Senior Portfolio Director

PAREXEL International

Day One- Wednesday 7th December 2011, 12.30pm

Choices and challenges in post approval studies
Jeff Trotter speaking at Late Phase Drug Development World Europe 2011

Jeff Trotter

Executive Vice President - Phase IV

PharmaNet/i3

Day One- Wednesday 7th December 2011, 9am

Opening remarks from the chair

Day Two- Thursday 8th December 2011, 10.15am

Observational Research – Areas of Consensus and Divergence

Dr. Florian Turk

Executive Director, Global Head Health Economics & Outcomes Research, Cardiovascular and Metabolism Business Franchise

Novartis Pharma AG

Dr. Florian Turk is Executive Director and Global Head Health Economics & Outcomes Research, Cardiovascular and Metabolism Business Franchise, Global Product Strategy & Commercialization at Novartis Pharma AG in Basel, Switzerland. Dr. Florian Turk is an experienced...

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Chris Twelves

Professor and Honorary Consultant in Medical Oncology

University of Leeds

Dr Lesley Wise

Senior Director, Global PV Risk Management

Takeda

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Late Phase Drug Development World Europe 2011 is a multi-faceted event

  • A two day conference
  • A showcase
  • Case studies by industry professionals
  • Speed networking
  • Interactive panel discussions
  • Roundtable brainstorms
  • Live debates

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You may also like to attend:

  • Late Phase Drug Development World Americas  
  • World Drug Safety Congress Europe
  • World Drug Safety Congress Americas
  • Clinical Outsourcing World Europe 

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We run training courses on:

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