IDMP Webinar Series -1 скачать в хорошем качестве

IDMP Webinar Series -1

IDMP Webinar Series – Episode 1 | Watch the Full Recording 🎥 Watch the recording to gain valuable insights into how IDMP (Identification of Medicinal Products) and GSRS (Global Substance Registration System) are transforming global regulatory data management, interoperability, and product traceability. This foundational webinar brings together global experts to explain why IDMP and GSRS are becoming essential pillars in digital regulatory transformation. 💡 What You’ll Learn In this 90-minute session, leading industry and regulatory experts cover: 🔹 Pharmaceutical Product Data Interoperability A global approach to standardized medicinal product data and why harmonization is critical. Speaker: Christian Hay 🔹 GSRS & UNIIs Understanding the Unique Ingredient Identifier (UNII) system, substance registration, and their impact on regulatory submissions. Speaker: Dr. Marlene Kim 🔹 IDMP & GSRS Foundations How ISO-based standards enhance data quality, safety, and compliance—and power seamless regulatory data exchange. 🔹 Global Implementation Best Practices Real-world updates from regulators including EMA, FDA, and MEB, with examples of how organizations are adopting IDMP/GSRS. 🔹 Expert Panel Discussion Featuring insights from GS1, Pistoia Alliance, Uppsala Monitoring Centre, CBG-MEB, and others on challenges, opportunities, and the future of IDMP. 🎯 Who Should Watch This Perfect for professionals in: Regulatory Affairs & CMC Pharmacovigilance & Drug Safety Global Regulatory Agencies Data Standards & Master Data Management IT & Digital Transformation in Pharma Product Lifecycle & Submission Teams Generic and Innovative Pharma Organizations 🌍 Why This Webinar Matters The pharma industry is rapidly shifting toward data standardization, transparency, and harmonized submissions. This session provides: Practical understanding of IDMP and GSRS Strategies to resolve technical and organizational challenges Insights on improving data quality and reducing submission errors Guidance from global experts actively shaping regulatory frameworks 🎙 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, Global Value Web 📥 Don’t miss this chance to learn directly from leaders driving the future of regulatory data exchange and IDMP adoption. 👉 Watch now and share with your teams!