Join Celegence at the Global Pharmaceutical Regulatory Affairs Summit (GPRAS) 2024

Celegence is proud to sponsor the Global Pharmaceutical Regulatory Affairs Summit (GPRAS) 2024, happening from October 22-24, 2024 in Brussels. As regulatory complexities continue to grow, this event is the ideal platform to meet our team and discover how our pharmaceutical solutions can help you navigate evolving global regulatory requirements. Visit us at Booth #3 to discuss your specific challenges and explore tailored solutions for compliance, submissions, and RIM management.

Join Hans van Bruggen, Celegence’s Chief Scientific Officer, on Day 2 | Tuesday, 22 October 2024, 9:40 – 10:10 CET for a session on “Facilitating the Digital Transformation of Module 3 to PQCMC, IDMP, and ICH M4Q R2“. Hans will cover practical strategies for modernizing regulatory submissions, ensuring alignment with the latest global standards.

Key points to be covered include:

• Simplifying the transformation of Module 3 to meet PQCMC and IDMP requirements
• Best practices for managing submissions across global markets under the ICH M4Q R2 guidelines
• Streamlining the connection between regulatory data, documents, and dossiers

Learn more about this session here: Facilitating the Digital Transformation of Module 3.

Our experts – Matt Tyler, Yusuf Leenen, Kosta Uzelac, Hans van Bruggen, and Rosal Khoury – will be at Booth #3 throughout the event. They’re ready to share insights on how Celegence’s services, from Regulatory Information Management (RIM) to medical writing and publishing, can help you streamline compliance and submissions processes.

At GPRAS 2024, attendees will engage with leaders in regulatory affairs, receive critical updates, and explore innovative solutions for navigating global regulatory markets. Key topics include:

• Regulatory Information Management
• Global eSubmissions
• Legislative Landscape and Regulatory Guidance
• Regulatory Affairs in Global Markets

Register here: Global Pharmaceutical Regulatory Affairs Summit 2024.

Celegence provides regulatory consulting services and solutions designed to meet the operational and strategic needs of pharmaceutical companies. Whether you’re looking for expertise in RIM data management, medical writing, or global submissions, we can assist you in maintaining compliance and reducing operational burdens.

Download our comprehensive services brochure to explore how Celegence can support your regulatory journey.

Meet our team for personalized consultations at Booth #3. For more information, contact info@celegence.com or simply stop by during the event.

• When: October 22-24, 2024
• Where: Sheraton Brussels Airport, Brussels
• How to Register: GPRAS 2024 Registration