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| 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 |