The Pharmacovigilance Podcast

By Julia Appelskog

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Category: Medicine

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Episodes: 24

Description

The Pharmacovigilance Podcast is your gateway to understanding how technology, regulation, and innovation converge to safeguard patient safety. Our discussions span legislative updates and the practical application of AI in pharmacovigilance workflows. Stay ahead of the curve with The Pharmacovigilance Podcast, where safety meets innovation.

Episode Date
Human in the Loop
May 08, 2026
From Finance to Pharmacovigilance: Lessons from Two Regulated Worlds
Mar 13, 2026
Transforming Benefit-Risk Assessment with AI
Feb 10, 2026
Inside PV Quality System: From Reactive QMS to AI-Supported Audits
Feb 02, 2026
From Freelancer to Award-Winning Founder: How to Build a Thriving Business in Pharma
Dec 19, 2025
MedDRA Matters: Behind the Scenes of International Standards
Dec 08, 2025
E2D(R1) Explained: Modern Safety Data Management Unpacked
Nov 26, 2025
Risk-Based Auditing in Pharmacovigilance: What Changes with EU Regulation 2025/1466?
Nov 06, 2025
Inside XEVMPD: Data, Safety and Strategy
Sep 25, 2025
The new CRO Business Playbook in the Age of AI
Sep 11, 2025
AI-Powered Literature Monitoring in Drug Safety
Sep 03, 2025
Clinical Trial Safety Reporting: What the 2025 UK Regulations Mean for You
Aug 29, 2025
EU Pharmacovigilance Regulation 2025/1466: Key Changes Explained
Aug 05, 2025
What Changed for UK Medicines After the Windsor Framework?
Jun 07, 2025
Data Protected: Inside EMA & OMS
May 28, 2025
The AI Safety Shift — EMA’s 2025–2028 Agenda
May 08, 2025
EMA Guidance on Anonymisation and Redaction of RMPs
Apr 25, 2025
EU Clinical Trials Regulation: The Full Implementation of the EU CTR
Feb 04, 2025
Navigating ICH E6(R3)
Jan 31, 2025
IRIS Transition simplified: Practical Guidance for MAHs
Dec 27, 2024
A New Era For Drug Safety
Dec 25, 2024
Roadmap to Regulatory Excellence in Pharmacovigilance
Dec 03, 2024
EMA AI Workshop: Safe & Responsible AI Use in PV
Nov 28, 2024
The AI Act: What It Means for Pharmacovigilance
Nov 26, 2024