From Awareness to Action

Strengthening Pharmacovigilance Through Adverse Event Reporting

ANNOUNCEMENTS

10/5/20261 min read

One adverse event report may look like a single case.

But when it is reported, assessed, and connected to other safety data, it can reveal a signal—and help protect thousands of patients.

Continuing PHARADA’s Webinar Series, we are pleased to present our next timely topic:

🔹 From Awareness to Action: Strengthening Pharmacovigilance Through Adverse Event Reporting

Join Dr. Alaa AlDabbas and Dr. Ala Esaifan, Clinical Safety and Pharmacovigilance professionals and Co-Founders of Inspire Pharma Consultancy, for a practical discussion on how effective adverse event reporting supports stronger safety systems throughout the product lifecycle.

The session will cover:

• Essential pharmacovigilance concepts and reporting principles
• Adverse event case management
• Literature monitoring and signal detection
• Special reporting situations
• Pharmacovigilance audit and inspection readiness

📅 Wednesday, 7 October 2026
🕑 12:00 PM – Jordan Time
💻 Online via Microsoft Teams
🎟️ Free attendance | Registration required

Whether you work in Pharmacovigilance, Clinical Research, Regulatory Affairs, Quality, Medical Affairs, or the wider pharmaceutical industry, this session will connect everyday reporting practices with their most important outcome: patient safety.