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Pharmacovigilance Europe 2016

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Date: 24-May-16 to 25-May-16
Location: The Kensington / London / United Kingdom
Category: Healthcare & Pharmaceuticals Conferences & Trade Fairs

The conference will bring together industry experts and regulators to discuss the new updates in EU legislation, operational challenges of implication of these changes, experience of implementing global risk management plans, the best and effective way forward, impact of IT and social media on PV and harmonization of different regulatory bodies.

After the outstanding success of Pharmacovigilance Europe 2015 bringing together busy PV professionals from around the world. It’s indeed a great pleasure once again to welcome all to Pharmacovigilance Europe 2016 for networking and knowledge sharing.

Key Themes
Explore the impact of PV legislation changes and updates on industries and the best practices
Assuring Compliance and its monitoring
Preparing for PV audit and inspections and the role of QPPV
Risk management plans, strategies and new risk- benefit analysis tools to improve REMS reporting
Implementing risk management and safety surveillance methodologies for medical devices
New approaches for risk minimization and communication
Determining steps and strategies for more transparency and involvement of patients
Discussing the how IT and Social media effect Pharmacovigilance and Adverse events reporting
Discuss and review the use of databases and emerging tools for generation and detection of safety signals
Importance of outsourcing and its effectiveness
Harmonization of regulatory framework- developed and emerging markets

Exhibitors

Dr Pipasha Biswas, Dr Heike Schoepper, Dr Shelley Gandhi, Nawab Qizilbash, Giovanni Furlan, Mircea Ciuca, Benedicte Lunddahl, Chetan Shatapathy

Go to event website