LexisNexis Reed Tech
Webinars
Stay ahead with LexisNexis Reed Tech webinars on Pharmaceutical & Medical Device regulations.
ON DEMAND WEBINAR
EUDAMED UDI Compliance: Why “Later” is Already Too Late
With the final phase of EUDAMED UDI implementation looming, the myth of “more time” is putting manufacturers at risk. The recent 3-month delay is not a grace period — it’s a wake-up call. If you haven’t already submitted to EUDAMED, you’re not just behind schedule — you’re in jeopardy of noncompliance.
In this timely webinar, we’ll break down what the delay actually means, how the window for smooth submissions is closing, and why voluntary uploads are now essential — not optional. Join us to uncover:
- Why waiting for the last moment is a high-risk strategy — and how it can compromise market access
- What real-world submission bottlenecks and system slowdowns already looked like in July 2025
- How to leverage voluntary submission as a critical dry run to debug your processes
- What successful manufacturers are doing now to scale up their UDI operations for EUDAMED
- How aligning your UDI data with broader global compliance goals (FDA GUDID, China NMPA, Korea MFDS) supports long-term efficiency
You’ll hear directly from our expert panel — including members of our product development team who actively serve on key industry committees shaping EUDAMED compliance. Their first-hand insights will help you navigate the latest regulatory expectations and avoid common pitfalls during implementation.
We’ll also share lessons learned from over 10,000 UDI records already submitted to EUDAMED and provide practical steps you can take immediately to accelerate your submission readiness — from data validation to internal system mapping.
Who Should Attend:
Regulatory affairs professionals, compliance managers, quality assurance teams, IT/data leads, and manufacturers responsible for UDI readiness in the EU.
Key Takeaway:
Starting today isn’t being early — it’s the last responsible moment. Don’t be caught in the final-hour scramble. Be part of the solution.
Register to our on-demand webinar
EUDAMED UDI Compliance:
Why “Later” is Already Too Late
Panelist
John Lorenc is the Director of Product Management at LexisNexis Reed Tech, specializing in delivering innovative solutions that address complex regulatory product data submission requirements for the Life Sciences industry, including both pharmaceuticals and medical devices. With a strategic focus on compliance, efficiency, and customer success, John leads the development and optimization of products that empower organizations to meet evolving global regulatory standards with confidence. Drawing on deep industry expertise and a passion for solving critical data challenges, John partners closely with regulatory, technical, and business stakeholders to ensure solutions not only meet compliance demands but also drive operational excellence.
Rob Leonetti is a passionate, global strategic business development leader and alliance director with over 20 years of experience in life sciences and healthcare, consistently delivering impactful results and client satisfaction. Success has been achieved through effective partnering with clients to understand their requirements, challenge the status quo and provide transformational, regulatory technology and professional services to accomplish business challenges and drive growth objectives. Rob’s skillsets include, product marketing, team leadership and building strategic alliance programs that accelerate organizational growth.
Grace Min is an accomplished Senior Product Manager with over 18 years at LexisNexis Reed Tech, specializing in life sciences data management, business analysis, and regulatory information solutions. She has played a pivotal role in guiding projects through their full lifecycle, ensuring alignment with client requirements, system usability, and operational efficiency. With deep expertise in process analysis, requirements gathering, and solution design, Grace is recognized for her ability to bridge the gap between technical teams and business stakeholders—consistently delivering solutions that enhance compliance, streamline workflows, and drive value for the life sciences industry.