9th Annual Risk Management and Pharmacovigilance Summit

In today’s fast changing and unforeseeable times, pharmaceutical companies need to follow a wide range of processes and stick to the majority of regulations, in order to ensure their pharmacovigilance is up to standards. But how to be in charge of the key component of effective drug regulation systems? The answer would be easy, well known as a PV.

Pharmacovigilance is the beating heart of pharmaceutical production. Without it, there would be no way to assess the effectiveness of drugs in comparison to their side effects. Especially today, when the pandemic is having a profound effect on the lives of millions of people around the world and the threat of disease and increasing casualties are destabilising every single industry, it’s important to protect the patients and enable the dissemination of knowledge amongst professionals to minimise the risk of adverse events. Let us see and reveal more what is hidden beyond the “unknown” of drug safety world.

The 9th Annual Risk Management and Pharmacovigilance Summit has been designed to embrace all the current topics and challenges that are important to explore and find the answers on how to embark the patients on the pharmacovigilance ships, what are the advances in structured benefit-risk assessment, what are the effective tools in signal detections, what are types of data available for predictive approaches, how to trust Artificial Intelligence for bias-free identification of risk factors for ADRs and many more. At this 9th Annual Risk Management and Pharmacovigilance conference you will hear 16+ real-life case studies and you have a chance to meet C-level representatives of leading pharma companies that have managed to provide the best safety measures to their patients in recent years.

This interactive pharma meeting will provide you with lessons learned and valuable tips shared by top players in the field. You will also benefit from remarkable networking opportunities due to limited seats of this business event. It is the right place for sharing ideas, getting insights and inspiration, learning from experienced leaders and establishing important business contacts valuable for your next future business path!

Join us and register today

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Key speakers

Andreas <b>OSANGER</b>


Director - Therapeutic Area Lead Nephrology
Monika <b>MANSKE</b>


Lead Quality Management and Deputy EEA QPPV
Victoria <b>BARTASEK</b>


Senior Associate Director, Global Pharmacovigilance
Stephanie <b>TCHERNY</b>

Stephanie TCHERNY

Global Head of Benefit-Risk Evaluation
Lisa <b>STAGI</b>


Drug Safety & Quality Head
Yvonne <b>NANCIU</b>


Country Head Pharmacovigilance

Key topics

  • How to effectively manage the adverse event data from digital initiatives?
  • What are the recent advances in Benefit-Risk field?
  • How patient safety could be more patient centric?
  • How to handle audits in remote conditions (Covid-19)?
  • The importance of involvement of patients in PV activities

Who Should Attend

Members of board, C-level, Senior/Global Vice Presidents, Directors, Heads of departments from pharma industry involved in:

  • Pharmacovigilance
  • Risk Management
  • PV Monitoring
  • Signal Detection
  • Data Collection
  • Patient Safety
  • Drug Safety
  • Benefit-Risk Evaluation
  • Quality Assurance
  • Reporting and Data Collection
  • Compliance
  • Inspections
  • Management Safety Data
  • Lifecycle Management Quality
  • Clinical Safety