The Pharmacovigilance Podcast
The Pharmacovigilance Podcast is your gateway to understanding how technology, regulation, and innovation converge to safeguard patient safety.
Our discussions span legislation updates and AI's practical application in pharmacovigilance workflows.
Stay ahead of the curve with The Pharmacovigilance Podcast – where safety meets innovation.
Latest Episode
From Freelancer to Award-Winning Founder: How to Build a Thriving Business in Pharma (19.12.2025)
Previous Episodes
- MedDRA Matters: Behind the Scenes of International Standards
- E2D(R1) Explained: Modern Safety Data Management Unpacked
- Risk-Based Auditing in Pharmacovigilance: What Changes with EU Regulation 2025/1466?
- Inside XEVMPD: Data, Safety and Strategy
- The new CRO Business Playbook in the Age of AI
- AI-Powered Literature Monitoring in Drug Safety
- Clinical Trial Safety Reporting: What the 2025 UK Regulations Mean for You
- EU Pharmacovigilance Regulation 2025/1466: Key Changes Explained
- What Changed for UK Medicines After the Windsor Framework?
- Data Protected: Inside EMA & OMS
- The AI Safety Shift — EMA’s 2025–2028 Agenda
- EMA Guidance on Anonymisation and Redaction of RMPs
- EU Clinical Trials Regulation: The Full Implementation of the EU CTR
- Navigating ICH E6(R3)
- IRIS Transition simplified: Practical Guidance for MAHs
- A New Era For Drug Safety
- Roadmap to Regulatory Excellence in Pharmacovigilance
- EMA AI Workshop: Safe & Responsible AI Use in PV
- The AI Act: What It Means for Pharmacovigilance
