About the Webinar

The 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.

Key Highlights

• Introduction to IDMP & GSRS: Understand the foundational concepts of these frameworks and their role in standardizing medicinal product data.
• Standardized Substance Descriptions: Learn how IDMP and GSRS provide precise scientific descriptions for substances, including impurities, metabolites, starting materials, and synthetic intermediates.
• Data Interoperability: Discover how these frameworks facilitate seamless data exchange among regulators, manufacturers, and distributors, improving pharmacovigilance and addressing drug shortages.
• Global Implementation Insights: Gain insights into the global adoption of IDMP and GSRS, including updates from regulatory bodies like the EMA and FDA.

🧑‍🎓𝐖𝐇𝐎 will benefit from this webinar?

• CMC – Regulatory Affairs professionals
• International regulators
• Industry experts in data standards and pharmacovigilance
• IT professionals involved in electronic regulatory submissions
• Anyone involved in the lifecycle of medicinal products within generic pharmaceutical companies.

🚨𝐖𝐇𝐘 do you need to attend this Webinar?

• Enhanced Regulatory Compliance: Stay updated on the latest regulatory requirements and best practices.
• Improved Data Management: Learn strategies to streamline data exchange and improve product safety.
• Networking Opportunities: Connect with industry experts and peers working on data standards and pharmacovigilance.
• Enhance 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

Are you struggling with:

• Complex Implementation Process
• Technical Challenges
• Regulatory and Organizational Alignment
• Resource Constraints
• Data Collection and Quality

𝐁𝐘 𝐓𝐇𝐄 𝐄𝐍𝐃 𝐎𝐅 𝐓𝐇𝐈𝐒 𝐖𝐄𝐁𝐈𝐍𝐀𝐑 𝐘𝐎𝐔 𝐔𝐍𝐃𝐄𝐑𝐒𝐓𝐀𝐍𝐃:

• Comprehensive Understanding of IDMP & GSRS
• Knowledge of Standardized Substance Descriptions
• Data Interoperability Insights
• Regulatory Compliance and Best Practices
• Networking Opportunities
• Global Implementation Insights

Free Registration: Click to reserve your seat!

After registering, you will receive a confirmation email containing information about joining the webinar.

The webinar is FREE to attend. No fees, just expert insights to optimize your lab!

Register now and secure your spot in our webinar!