Webinar: Creating a More Intelligent Pharmaceutical Industry: Enabling Regulatory Data Exchange Series-1

Posted May 8, 2025

“Creating a More Intelligent Pharmaceutical Industry: Enabling Regulatory Data Exchange Series-1”.

🎥 Watch the Recording Now to gain valuable insights into how IDMP (Identification of Medicinal Products) and GSRS (Global Substance Registration System) are transforming the way regulatory data is managed, shared, and interpreted globally.

💡 What You’ll Learn:

This 90-minute session features global thought leaders and industry experts discussing:

Pharmaceutical Product Data Interoperability: A global approach to standardized medicinal product data (Speaker: Christian Hay).
GSRS & UNIIs: Understanding unique ingredient identifiers and their critical role in regulatory submissions (Speaker: Marlene Kim).
IDMP & GSRS Foundations: How these ISO-based frameworks improve data interoperability, enhance drug safety, and support regulatory compliance.
Global Implementation Best Practices: Updates and use cases from regulatory bodies including EMA, FDA, and MEB.
Panel Discussion: In-depth perspectives from experts at GS1, Pistoia Alliance, Uppsala Monitoring Centre, CBG-MEB, and others.

🎯 Who Should Watch:

This webinar is essential for:

Regulatory Affairs & CMC professionals
Global health regulators
Pharmacovigilance & data standardization experts
IT professionals in regulatory submissions
Generic pharma professionals managing product lifecycle data

🌍 Why It Matters:

The pharmaceutical industry is under pressure to improve regulatory transparency, data quality, and product traceability. This webinar equips you with:

Practical knowledge of IDMP and GSRS standards
Strategies for handling technical and organizational challenges
Insights on overcoming data quality and resource constraints
Direct access to expert commentary and global case studies

🎙 Speakers:

Christian Hay – Sr. Consultant Healthcare, GS1 Global Office | ISO TC/215 WG6 Convenor
Dr. Marlene Kim – Chemist & GSRS Consultant

🧠 Expert Panelists:

Jean-Gonzague Fontaine | Olof Lagerlund | Birthe Nielsen | Egor Puzanov | Marcel Hoefnagel
Moderator: Louis Hendriks, CEO & Founder – GVW

📥 Don’t miss this opportunity to learn from global experts shaping the future of pharmaceutical regulation and data exchange.

👉 [Watch the webinar recording now]

Click on the link below to watch the full video (Part 1 with Louis, Birthe,Christian)!

Click on the link below to watch the full video(Part 2 with Marlene and Panel Discussion)!