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DTSTART;TZID=UTC:20250506T173000
DTEND;TZID=UTC:20250506T190000
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SUMMARY:Webinar: Creating a More Intelligent Pharmaceutical Industry: Enabling Regulatory Data Exchange Series
DESCRIPTION:[vc_row][vc_column][mk_image src=”https://global-value-web.com/wp-content/uploads/2025/04/gvw-webinar-linkedin-event-banner-16x9_1920x1080px_v2-2.jpg” image_size=”full” link=”https://events.teams.microsoft.com/event/99a7abea-3eb9-482d-809c-0fc9d06d9c46@75b9c69a-f477-4f9c-bfd4-c659559b92a6″ margin_bottom=”20″][vc_row_inner][vc_column_inner][vc_column_text css=”.vc_custom_1745582676604{margin-bottom: 0px !important;}”]\nAbout the Webinar\nThe first instalment of our comprehensive webinar series to explore the cutting-edge frameworks revolutionising pharmaceutical regulatory data exchange: Identification of Medicinal Products (IDMP) and Global Substance Registration System (GSRS). These ISO-based standards are transforming how medicinal product information is shared globally, enhancing patient safety and operational efficiency.\nKey Highlights\n\nIntroduction to IDMP & GSRS: Understand the foundational concepts of these frameworks and their role in standardizing medicinal product data.\nStandardized Substance Descriptions: Learn how IDMP and GSRS provide precise scientific descriptions for substances, including impurities, metabolites, starting materials, and synthetic intermediates.\nData Interoperability: Discover how these frameworks facilitate seamless data exchange among regulators, manufacturers, and distributors, improving pharmacovigilance and addressing drug shortages.\nGlobal Implementation Insights: Gain insights into the global adoption of IDMP and GSRS, including updates from regulatory bodies like the EMA and FDA.\n\n🧑‍🎓𝐖𝐇𝐎 will benefit from this webinar?\n\nCMC – Regulatory Affairs professionals\nInternational regulators\nIndustry experts in data standards and pharmacovigilance\nIT professionals involved in electronic regulatory submissions\nAnyone involved in the lifecycle of medicinal products within generic pharmaceutical companies.\n\n🚨𝐖𝐇𝐘 do you need to attend this Webinar?\n\nEnhanced Regulatory Compliance: Stay updated on the latest regulatory requirements and best practices.\nImproved Data Management: Learn strategies to streamline data exchange and improve product safety.\nNetworking Opportunities: Connect with industry experts and peers working on data standards and pharmacovigilance.\nEnhance Drug Safety and Traceability: Learn how IDMP compliance enhances drug safety through improved traceability and pharmacovigilance, ensuring that your products meet the highest safety standards\n\nAre you struggling with:\n\nComplex Implementation Process\nTechnical Challenges\nRegulatory and Organizational Alignment\nResource Constraints\nData Collection and Quality\n\n𝐁𝐘 𝐓𝐇𝐄 𝐄𝐍𝐃 𝐎𝐅 𝐓𝐇𝐈𝐒 𝐖𝐄𝐁𝐈𝐍𝐀𝐑 𝐘𝐎𝐔 𝐔𝐍𝐃𝐄𝐑𝐒𝐓𝐀𝐍𝐃:\n\nComprehensive Understanding of IDMP & GSRS\nKnowledge of Standardized Substance Descriptions\nData Interoperability Insights\nRegulatory Compliance and Best Practices\nNetworking Opportunities\nGlobal Implementation Insights\n\n[/vc_column_text][vc_btn title=”Register Now” shape=”square” color=”warning” size=”lg” link=”url:https%3A%2F%2Fevents.teams.microsoft.com%2Fevent%2F8c7eb69c-1a30-4e31-a688-10edb8b8956c%4075b9c69a-f477-4f9c-bfd4-c659559b92a6|title:Register%20Now|target:%20_blank|”][vc_column_text css=”.vc_custom_1746180659612{margin-bottom: 0px !important;}”]\nFree Registration: Click to reserve your seat! ( https://events.teams.microsoft.com/event/99a7abea-3eb9-482d-809c-0fc9d06d9c46@75b9c69a-f477-4f9c-bfd4-c659559b92a6 )\nAfter registering, you will receive a confirmation email containing information about joining the webinar.\nThe webinar is FREE to attend. No fees, just expert insights to optimize your lab!\nRegister now and secure your spot in our webinar![/vc_column_text][/vc_column_inner][/vc_row_inner][/vc_column][/vc_row]\n
URL:https://events.teams.microsoft.com/event/8c7eb69c-1a30-4e31-a688-10edb8b8956c@75b9c69a-f477-4f9c-bfd4-c659559b92a6
CATEGORIES:Recent Events
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