Opus Regulatory — Washington, DC | October 20 We'll be at Opus Regulatory's Global Labeling and Regulatory Symposium in Washington, DC. Come find our team to discuss how LexisNexis supports...
Regulatory Affairs Professionals Society — Charlotte, North Carolina | September 15–17 Meet us at RAPS Convergence 2026 in Charlotte — the flagship event for regulatory affairs professionals...
Informa Connect — Berlin, Germany | June 15–18 Find us at the MedTech Summit in Berlin, where regulatory affairs professionals and industry leaders tackle MDR/IVDR compliance and market access...
Drug Information Association — Philadelphia, Pennsylvania | June 14–18 We'll be at the DIA Global Annual Meeting in Philadelphia among thousands of life sciences professionals. Visit...
Drug Information Association — North Bethesda, Maryland | February 2–4 Join us at the DIA RSIDM Forum in North Bethesda. Connect with our team to see how LexisNexis helps life sciences organizations...
As regulatory authorities and health systems push toward digital transformation, Fast Healthcare Interoperability Resources (FHIR) is emerging as a key framework for enabling the exchange of health data—including product labeling information.
In this webinar, experts from LexisNexis® Life Sciences Solutions, a recognized thought leader in regulatory data standards and electronic labeling (eLabeling), will break down the implications of FHIR for medical device and pharmaceutical manufacturers. From enhancing eLabeling to streamlining updates across jurisdictions, FHIR is set to transform how labeling content is created, managed, and delivered.
Whether you’re just starting to assess FHIR’s relevance to your organization or are looking to optimize digital labeling strategies, this session will provide actionable insights from the team helping shape the future of health data standards.
Robin Schilling As Head of Regulatory Compliance Services for LexisNexis Life Sciences Solutions, Robin drives innovation, strategic planning, and cross-functional collaboration across life sciences and global markets. With expertise in regulatory strategy, stakeholder engagement, and risk management, she builds global teams and positions organizations for long-term success.
Sam Thompson As an Independent Consultant, Sam leverages his extensive background in pharmaceutical data architecture to provide tailored solutions that meet the specific needs of his clients. He specializes in designing and implementing data strategies that ensure compliance, scalability, and operational efficiency in pharmaceutical organizations.
Mike Baird As the Director of Product Management for Schlafender Hase, Mike has built his career at the intersection of product management and business development, shaping software solutions that solve user problems and address market needs. With over 30 years of international business experience spanning life sciences, healthcare, enterprise software, and SaaS, he has led global accounts across North America, EMEA, and APAC.
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