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
Clinical Trial Safety Reporting: What the 2025 UK Regulations Mean for You (29.08.2025)
Previous Episodes
- EU Pharmacovigilance Regulation 2025/1466: Key Changes Explained 05.08.2025
- What Changed for UK Medicines After the Windsor Framework? 07.06.2025
- Data Protected: Inside EMA & OMS 28.05.2025
- The AI Safety Shift — EMA’s 2025–2028 Agenda 08.05.2025
- EMA Guidance on Anonymisation and Redaction of RMPs 25.04.2025
- EU Clinical Trials Regulation: The Full Implementation of the EU CTR 04.02.2025
- Navigating ICH E6(R3) 31.01.2025
- IRIS Transition simplified: Practical Guidance for MAHs 27.12.2024
- A New Era For Drug Safety 25.12.2024
- Roadmap to Regulatory Excellence in Pharmacovigilance 03.12.2024
- EMA AI Workshop: Safe & Responsible AI Use in PV 28.11.2024
- The AI Act: What It Means for Pharmacovigilance 26.11.2024
