Conference Focus
Rapid growth of pharmaceutical industries has resulted in innovations and increase in the number of drugs into the market, which has also resulted in rise of adverse drug events and drug related toxicities. These events have led to a rise in public safety concerns, stringent regulatory policies, expectations and tough inspection regimes, providing the much needed stimulation for the growth of pharmacovigilance market. Recently, the scope of drug safety reporting has been extended to medical devices, traditional medicines and biologics. Global pharmacovigilance market is estimated to touch a market value of $5,008.2 million in 2019.
The Pharmacovigilance Europe 2016 conference will participants an opportunity and a platform to share experiences with the likeminded individuals in the field. The conference will also provide an insight into the complexities and challenges impacting public safety and risk management, focusing mainly on drugs, biologics and medical devices and the future of PV in the globalization era.
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 professionals from over ~48 companies around the world. It’s indeed a great pleasure 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
Why Should You Attend
Pharma/BioTech companies are always faced with the challenge to improve quality of the safety data with the ever-increasing quantity of the data. The companies are also left with the challenge to manage the dynamic regulatory requirements. There are still many complexities that the industries and the regulatory authorities have to tackle. With more communication and networking you can expand your knowledge on the key complications currently experienced by various industries and departments and design new strategies to overcome the same.
Who Should Attend
VPs, Directors, Heads, Managers, Scientific Advisors, Consultants, Research Scholars and professionals with intermediate to advance knowledge and experience in the following
Pharmacovigilance
Risk management
Drug safety
Pharmacoepidemiology
Drug Research & Development
Clinical Pharmacology
Clinical Safety
Information and Clinical Data Management
Medical product safety assessment
Clinical research & safety
Data analysis
Information technology
Medical information
Health outcomes
Sales and Marketing
Clinical Trials & CRO’s
Contract Manufacturing
For more
Rapid growth of pharmaceutical industries has resulted in innovations and increase in the number of drugs into the market, which has also resulted in rise of adverse drug events and drug related toxicities. These events have led to a rise in public safety concerns, stringent regulatory policies, expectations and tough inspection regimes, providing the much needed stimulation for the growth of pharmacovigilance market. Recently, the scope of drug safety reporting has been extended to medical devices, traditional medicines and biologics. Global pharmacovigilance market is estimated to touch a market value of $5,008.2 million in 2019.
The Pharmacovigilance Europe 2016 conference will participants an opportunity and a platform to share experiences with the likeminded individuals in the field. The conference will also provide an insight into the complexities and challenges impacting public safety and risk management, focusing mainly on drugs, biologics and medical devices and the future of PV in the globalization era.
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 professionals from over ~48 companies around the world. It’s indeed a great pleasure 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
Why Should You Attend
Pharma/BioTech companies are always faced with the challenge to improve quality of the safety data with the ever-increasing quantity of the data. The companies are also left with the challenge to manage the dynamic regulatory requirements. There are still many complexities that the industries and the regulatory authorities have to tackle. With more communication and networking you can expand your knowledge on the key complications currently experienced by various industries and departments and design new strategies to overcome the same.
Who Should Attend
VPs, Directors, Heads, Managers, Scientific Advisors, Consultants, Research Scholars and professionals with intermediate to advance knowledge and experience in the following
Pharmacovigilance
Risk management
Drug safety
Pharmacoepidemiology
Drug Research & Development
Clinical Pharmacology
Clinical Safety
Information and Clinical Data Management
Medical product safety assessment
Clinical research & safety
Data analysis
Information technology
Medical information
Health outcomes
Sales and Marketing
Clinical Trials & CRO’s
Contract Manufacturing
For more
