25th-26th of October 2023, Berlin, Germany

Unleash the Power of Pharmacovigilance and Risk Management at Our Exclusive Conference! Register Now to Stay Ahead in Adverse Event Reporting, Signal Detection, Risk Assessment, and Communication. Gain Valuable Insights, Network with Industry Leaders, and Boost Pharmaceutical Safety. Join Top Professionals for Unparalleled Knowledge and Strategic Connections. Don’t Miss Out!

Our summit is designed to help you

  • Gaining insights and knowledge of the latest advancements and best practices in pharmacovigilance
  • Learn the best practices for managing the safety and efficacy of pharmaceutical products
  • Stay up-to-date with regulatory requirements and compliances
  • Delve into topics such as adverse event reporting, signal detection, risk assessment, and risk communication
  • Connect with peers and learn from the industry’s top professionals
  • Benefit from tools and strategies to effectively manage pharmacovigilance

Meet the training speakers

FABIO DE GREGORIO

Vice President, Head of Drug Safety Europe, UK QPPV

PAV RISHIRAJ

Director, Head of Pharmacovigilance

GLORIA BUSTOS BUSTO

Senior Director, Head of Pharmacovigilance EMEA and APAC

DAWN MUCCI

Senior Manager, PV Alliance Management

BERT VAN LEEUWEN

Deputy Qualified Person for Pharmacovigilance (QPPV)

WIVINA DE WAELE

Sr. Director Safety Lead EU, Global Patient Safety

Key Topics

Digital Transformation and Automation in Pharmacovigilance

Use of Real-World Data (RWD) and Real-World Evidence (RWE) in Risk Management

Pharmacovigilance for Biologics and Biosimilars

Management of Medication Errors and Adverse Drug Reactions (ADRs)

Risk Communication and Patient-Centered Pharmacovigilance

Artificial Intelligence (AI) and Machine Learning (ML) in Pharmacovigilance

Regulatory Compliance and Good Pharmacovigilance Practices (GVP)

Who should attend

VPs, MDs, Global Heads, Directors, Department Heads and International Managers from Pharma industry involved in:

  • Pharmacovigilance professionals
  • Drug safety
  • Regulatory affairs
  • Medical professionals
  • Pharmaceutical and biotechnology
  • Contract research organizations (CROs)
  • Quality assurance and control
  • Clinical development and operations professionals
  • Healthcare compliance
  • Data and information management
  • Patient safety
  • Risk management and mitigation