Global Pharmacovigilance and Risk Management Summit

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

GLORIA BUSTOS BUSTO

Senior Director, Head of Pharmacovigilance EMEA and APAC

BERT VAN LEEUWEN

Deputy Qualified Person for Pharmacovigilance (QPPV)

PAV RISHIRAJ

Director, Head of Pharmacovigilance

DAWN MUCCI

Senior Manager, PV Alliance Management

WIVINA DE WAELE

Sr. Director Safety Lead EU, Global Patient Safety

Key Points

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

Register Now

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