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Drug Safety Data Collection & Evaluation

Event overview

This half day webinar will present a fresh and original perspective on one of the biggest challenges in the pharmacovigilance world today; gathering critical safety information throughout a drug's lifecycle, from various global departments and functions, and performing an integrated assessment on which to base future decisions.

Industry leaders, academia & regulators will review the latest alterations to the pharmaceutical business model made necessary by growing attention to drug safety concerns, evolving regulatory guidelines and the solutions to managing ever growing volumes of data with decreasing budgets and company sizes.

The webinar will concentrate on how data capture and management approaches can be better integrated into the company structure to aid safety decision making as well as minimise risks both to patients and the company.

By hearing from top figures in both industry & academic who are designing successful data systems for drug safety functions, participants will have access to vital information on lessons learned and effective models to be implemented into their own strategy.

Why Join?

  • Simplify decision making throughout a drug’s lifecycle by better data collection & evaluation.
  • Build superior drug safety systems and organisational structures to support quick and centralised decision making.
  • Clarify drug safety roles and responsibilities to enable comprehensive data collection and ensure effective analysis.
  • Discover how to develop strong relationships with external stakeholders and bring outsourced activities in line with company aims.
  • Learn from case studies recently implemented to address challenges in increasing data collection & quality.

Who Should Join?

VPs, Senior Directors and Mangers of:

Pharmacovigilance & drug safety, Data & Information Knowledge Management, Risk management, Medical product safety assessment, Data analysis, Epidemiology, Medical information, Global Information Solution (IS), Scientific Data Analysis, Information Specialists.

Your Prestigious Speaker Panel

PHARMA

Head of Data Management, Global Drug Safety, Global Regulatory Affairs, Drug Safety and Quality Assurance R&D
Grünenthal, Germany

Consultant Therapeutic Head Transplantation, Medical Affairs
Astellas Pharma Europe, UK
Ph.D Candidate
Sahlgrenska Academy,
University of Gothenburg, Sweden

EXPERT SOLUTION PROVIDER

Pharmacovigilance Manager
IRW Consulting, Sweden

ACADEMIA

Professor of Epidemiology, Department of Psychiatry
UMKC School of Medicine, USA

Department of Pharmacology
Universite Victor Segalen Bordeaux, France

Global Head of Safety Risk Management (PDS)
& EU-QPPVGlobal Head of Safety Risk Management (PDS) & EU-QPPV

 
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