Pharmacovigilance World 2026 Conference

We are delighted to welcome you to the Pharmacovigilance World 2026, and we are confident that your active participation will contribute to the advancement of drug safety practices. Together, let us strive towards a safer and more vigilant healthcare system that prioritizes patient well-being and ensures the continued benefit of medications worldwide.

As medical science advances, so does our understanding of drug safety and the need for vigilance when it comes to monitoring its usage. In recent years, pharmacovigilance has gained significant attention and importance due to the growing complexity of drug therapies, the emergence of new medicines, and the increased scrutiny of regulatory agencies. This has led to a greater emphasis on monitoring the safety profiles of pharmaceutical products throughout their lifecycle, from pre-marketing clinical trials to post-marketing surveillance.

The need for effective pharmacovigilance systems becomes even more crucial as the global population continues to expand, resulting in an increased consumption of medications. Adverse drug reactions (ADRs) can have severe consequences, leading to hospitalizations, prolonged treatments, and in some cases, even fatalities. Therefore, it is imperative to enhance our understanding of ADRs, identify potential risks, and implement appropriate risk mitigation strategies. To efficiently address these challenges, collaboration between international regulatory bodies, healthcare providers, and patients is essential. With a strong focus on patient safety as well as public health and by creating an interconnected network of experts from around the world who are dedicated to advancing our understanding of drug safety and pharmacovigilance, we can create a robust system.

This conference will serve as a knowledge-sharing and networking platform, providing a unique opportunity for researchers, pharmacists, healthcare professionals, industry representatives, and regulatory authorities to come together and discuss the latest trends, challenges, and advancements in pharmacovigilance. By sharing experiences and best practices, we aim to enhance global drug safety and improve patient outcomes. Throughout the conference, we will delve into various topics such as signal detection and management, adverse event reporting and analysis, risk assessment, benefit-risk evaluation, regulatory updates, collaboration and the integration of artificial intelligence and digital technologies in pharmacovigilance.

Our esteemed panel of speakers, comprising leading experts from academia, industry, and regulatory agencies, will present their research findings, share case studies, and engage in thought-provoking discussions. The conference will also feature interactive networking opportunities, fostering collaboration and enabling the exchange of ideas.

Conference Link: https://corvusglobalevents.com/conference/pharmacovigilance-world

Registration Link: https://corvusglobalevents.com/pharmacovigilance-world/registration

Key Highlights:

Signal Detection & Management

Regulatory Intelligence & Global Harmonization

Automation in Case Processing

Risk Management Plans (RMPs)

Benefit-Risk Evaluation

Post-Marketing Surveillance

PV Systems & Quality Management

PV Outsourcing & Vendor Oversight

Patient-Centric Drug Safety

Medical Device Safety & Combination Products

PV in Clinical Trials

Labeling and Safety Communication

AI/ML in Pharmacovigilance

Global Safety Databases & Data Standardization

PV Audits, Inspections & Readiness

Attendees includes VPs, GMs, Directors, Heads and Managers of

Pharmacovigilance & Drug Safety

Risk Management & Signal Detection

Regulatory Affairs & Regulatory Intelligence

Medical Affairs & Clinical Safety

Real-World Evidence & Post-Marketing Surveillance

Safety Systems & Data Analytics

Case Processing & Quality Assurance

Global Safety Compliance & Inspection Readiness

Medical Device Safety & Vigilance

Outsourcing & Vendor Management

Artificial Intelligence & Automation in PV

Safety Labeling & Product Information

Clinical Development & PV Integration

Biopharmaceuticals & Vaccines Safety

CROs, PV Vendors, and Consulting Firms

Regulatory Bodies, Health Authorities & HTA Agencies

Patient Safety Advocates & Healthcare Institutions

Academic Researchers & Industry Associations