Webinar: Creating a More Intelligent Pharmaceutical Industry: Enabling Regulatory Data Exchange Series-2
Creating a More Intelligent Pharmaceutical Industry: Enabling Regulatory Data Exchange – Series 2
Explore how the pharmaceutical industry is transforming regulatory data exchange through structured substance information and global data standards like IDMP and GSRS.
💡 What You’ll Learn:
This 90-minute session brings together leading experts to discuss substance registration systems, implementation best practices, and global collaboration:
🔸 Implementing SRS for IDMP Global Substance IDs (GSIsDs)
Speaker: Dr. Olof Lagerlund, Substance Expert, Uppsala Monitoring Centre
🔸 Leveraging on SRS within a Pharma Company – GSK Use Case
Speaker: Ian Mawer, Associate Director, GSK
💬 Panel Discussion follows the speaker sessions with expert insights on global adoption and challenges.
🎯 Who Should Watch:
This webinar is tailored for:
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Regulatory Affairs & CMC professionals
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Data Standards & Pharmacovigilance teams
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Pharma IT & Master Data Management leads
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Regulatory strategy experts and submission teams
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Stakeholders driving global compliance and IDMP readiness
🌍 Why It Matters:
With global regulatory alignment on the rise, this webinar provides:
✅ Practical insights into SRS and GSIsD adoption
✅ Real-world examples from GSK and Uppsala Monitoring Centre
✅ Guidance on overcoming data, technology, and implementation hurdles
✅ Direct access to global regulatory and pharma perspectives
🎙 Speakers:
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Dr. Olof Lagerlund, Uppsala Monitoring Centre
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Ian Mawer, GSK
Expert Panelists:
Christian Hay | Marleen Kim | Birthe Nielsen | Egor Puzanov | Marcel Hoefnagel
Moderator: Louis Hendriks, CEO & Founder – GVW
📥 Watch the Recording Now
Learn from global experts who are shaping the future of regulatory data interoperability and substance data exchange.
Click on the link below to watch the full video (Part 1)!
Click on the link below to watch the full video(Part 2 )!
