Global experts gather at the Pharmacovigilance and Drug Safety Summit 2025 to explore emerging trends, innovative practices, and regulatory updates, enhancing patient safety through collaboration and advanced pharmacovigilance strategies.
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
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
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