LexisNexis Reed Tech
Webinars
Stay ahead with LexisNexis Reed Tech webinars on Pharmaceutical & Medical Device regulations.
UPCOMING WEBINAR
FHIR and the Future of Labeling: What You Need to Know
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® Reed Tech, a recognized thought leader in regulatory data standards and digital labeling, will break down the implications of FHIR for medical device and pharmaceutical manufacturers. From enhancing electronic labeling (eLabeling) to streamlining updates across jurisdictions, FHIR is set to transform how labeling content is created, managed, and delivered.
We’ll explore:
- What FHIR is and how it’s being adopted in health authority systems globally
- How FHIR impacts Unique Device Identification (UDI) and structured product labeling (SPL)
- The role of FHIR in driving efficiency, traceability, and compliance
- Real-world examples of how Reed Tech is helping manufacturers prepare for a FHIR-enabled future
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.
Who should attend:
- Regulatory Affairs Professionals
- Labeling Managers
- Digital Transformation Leads
- IT Stakeholders
- Compliance Officers in the Medical Device and Pharma Sectors
Register to our Upcoming Webinar
FHIR and the Future of Labeling: What You Need to Know
Panelist
Robin Schilling
As Head of Regulatory Compliance Services for LexisNexis Reed Tech, 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 combined journey through product management and business development, shaping software solutions to both solve user problems and address market needs, while driving business growth.
He has worked across multiple verticals and industries—spanning packaging, print, design, graphics, digital, enterprise software, SaaS, life sciences/healthcare, branded FMCG/CPG, and retail.
With over 30 years of international business experience, Mike has led global business accounts and frequently traveled across North America, EMEA, and the APAC regions.