Celegence at RSIDM Forum 2025: Discover Our Tech-empowered Regulatory Services

Join us at the Regulatory Submissions, Information, and Document Management (RSIDM) Forum 2025, taking place February 3-5, 2025, at the Bethesda North Marriott Hotel and Conference Center, North Bethesda, Maryland, USA.

Visit us at Booth 106 to discover how our services are improved by advanced in-house technology and driven by experienced subject matter experts, enabling us to consistently deliver high-quality results more swiftly and cost-efficiently.

This premier event brings together industry professionals, regulatory thought leaders, and innovators in life sciences to explore the latest advancements and best practices in regulatory submissions, information, and document management. From networking opportunities to gaining actionable insights, the RSIDM Forum 2025 is the place to be for regulatory professionals.

Event Details:

• When: February 3 – 5, 2025
• Where: Bethesda North Marriott Hotel and Conference Center, 5701 Marinelli Road, North Bethesda, MD 20852, USA

Our team of experts will showcase cutting-edge tech-enabled solutions, publishing & submission services, and medical/technical writing support, all designed to meet the evolving needs of the pharmaceutical industry. Stop by our booth to learn how we can help you:

• Optimize Regulatory Submissions: Streamline your submission processes with our expertise and innovative tools like Dossplorer™ and Dosscriber™.
• Enhance Medical Writing: Deliver precise and compliant documents with our specialized medical and technical writing services.
• Leverage Technology: Harness the power of automation and AI to simplify complex regulatory workflows.

Connect with our experienced team members, including Punya Abbhi, Lakshmeenarayana Goundalkar, Hans van Bruggen, Kosta Uzelac, Matt Tyler, and John Popp, who will be available throughout the event to discuss your unique challenges and share insights.

Don’t miss the opportunity to engage in one-on-one consultations with our regulatory experts. Learn how Celegence can help you achieve compliance efficiently and effectively. Additionally, experience live demos of our proprietary tools, Dossplorer™ and Dosscriber™, to see how they can simplify and enhance your regulatory processes.

Visit us at Booth 106 to learn more about how Celegence can help you navigate the complexities of regulatory submissions, information, and document management. For more information, reach out to info@celegence.com or contact us online. We look forward to seeing you there!