Join Us @ RAPS Regulatory Convergence 2024

We are excited to announce Celegence’s premier sponsorship and participation at the RAPS Regulatory Convergence 2024 in Long Beach, California from 17-19 September 2024. As a leader in regulatory consulting, we are committed to driving innovation and compliance in the pharmaceutical, medical device and IVD industries. This year, Celegence will be at Booth 631 and is proud to sponsor an insightful session on harnessing the power of AI to maintain post-market clinical data efficiently, ensuring sustainable compliance with the EU MDR and IVDR.

Discover the innovation of our Celegence tech-enabled solutions, offering a strategic advantage in navigating the dynamic regulatory landscape of today’s competitive market.

Join Our Sponsored Presentation: “Maintaining Post-Market Clinical Data Efficiently with Technology (Automation/AI) for Sustainable MDR and IVDR Compliance”
Date and Time: 10:45 AM – 11:10 AM PDT | Wednesday, September 18, 2024

Location: Long Beach Convention & Entertainment Center 300 E Ocean Boulevard, Long Beach, CA 90802, USA

How to Register: click here

In today’s rapidly evolving regulatory landscape, maintaining up-to-date clinical data throughout a product’s lifecycle is more critical than ever. This session will explore the pivotal role of clinical data in gaining regulatory approval and ensuring market access for medical devices and IVDs. We will dive into how manufacturers can harness cutting-edge AI technology to streamline the updating and maintenance of clinical data during the post-market phase.

• Key Stages of a Product’s Lifecycle: Gain a comprehensive understanding of the clinical data required at each stage of a product’s lifecycle to support regulatory submissions.
• Leveraging Technology and AI: Discover how AI technology can be utilized to efficiently update clinical data, ensuring continuous compliance with regulatory requirements during the post-market phase.
• Benefits of AI in Clinical Data Management: Learn about the tangible advantages of integrating AI into clinical data management, including drafting and updating technical and clinical data in line with the expectations of competent authorities.

We are thrilled to have Joseph-Richardson Larbi, Director of Medical Device Regulatory Affairs at Celegence, as our featured speaker. With over two decades of experience in medical device regulatory affairs, Joseph specializes in the lifecycle management of medical devices and IVDs. His expertise spans across various therapeutic areas, including Diabetes, Ophthalmology, Nicotine Replacement Therapy (NRT), and Extracorporeal Membrane Oxygenation (ECMO). Joseph’s profound knowledge and practical insights make him an invaluable resource for professionals navigating the complexities of MDR and IVDR compliance.

The RAPS Regulatory Convergence is a premier event for regulatory professionals, offering unparalleled opportunities to connect, learn, and share knowledge with experts from around the globe. Be sure to visit us at Booth 631 and attend our session to discover how Celegence can help you navigate the complexities of post-market clinical data management using AI-driven solutions. Engage in meaningful discussions on how our innovative tech-enabled services revolutionize reliability, accelerate processes, and optimize costs in managing your regulatory affairs.

Secure your consultation slot by reaching out to us in advance at info@celegence.com, contact us online.

For more details about the event and to view the full agenda, visit the following link: RAPS Convergence 2024. We look forward to seeing you in Long Beach!