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Date
- Sep 16 2025
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3:00 PM – 4:30 PM, Central European Time (CET)
9:00 AM – 10:30 AM, Eastern Time (ET)
Overview
Are you ready to revolutionize your approach to regulatory compliance? Don’t miss our upcoming webinar where we dive deep into the essential features of EUDAMED that can transform your compliance strategies and boost your operational efficiency!
EUDAMED is reshaping how life sciences organizations manage regulatory data, device traceability, and clinical oversight. With full implementation deadlines approaching, the time to act is now. Many organizations are still grappling with unclear processes, fragmented data systems, and lack of integration: risking delays, penalties, or worse, market inaccessibility.
In this session, we will walk you through the core requirements of EUDAMED, the impact on industry roles, and most importantly — how to turn compliance into an opportunity for greater transparency, efficiency, and strategic advantage.
Speaker
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Darrius Kilpatrick
Darrius Kilpatrick is a Product Manager at Honeywell Life Sciences, specializing in complaint handling, quality systems, and regulatory compliance for the medical device industry. With over a decade of experience, he is a subject matter expert in ISO 14971, vigilance reporting, and root cause analysis, and has worked closely with FDA and other regulatory bodies.
At Honeywell, he leads product initiatives around TrackWise and TrackWise Digital, supporting organizations in achieving EU MDR and EUDAMED compliance. Darrius has a strong background in CAPA processes and complaint investigations, and has previously held key quality roles at Medtronic and L&T Technology Services.
Partner

Honeywell
Website
https://www.spartasystems.com/Honeywell brings leading-edge quality management solutions to regulated industries. With TrackWise® and TrackWise Digital®, Honeywell provides enterprise and cloud-based QMS software solutions that help companies go to market faster and deliver the highest standards for product quality, compliance, and customer satisfaction. Honeywell is an innovator in its field, driving smart quality with first-of-its-kind AI-enabled quality solutions. By applying the latest digital technologies, our products simplify the process of quality management and guide customers toward proactive quality. The combination of Sparta Systems and Honeywell brings together Sparta Systems’ quality management leadership with over 100 years of industrial and software expertise from Honeywell. Together, Sparta and Honeywell will shape the future of digital quality and operational excellence for the life sciences industry.
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Who Should Attend:
Life Sciences companies (Pharma, Biotech, med devices): Quality assurance, manufacturing professionals, Regulatory Affairs Managers, IT Administrators (Quality, Compliance), Management Executives, Clinical Research Coordinators
- Skill Level: Intermediate
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Topics:
Key EUDAMED Modules: Discover how to automate information exchange with the Machine to Machine (M2M) interface, manage device safety and regulatory compliance utilizing the Vigilance module, efficiently register Unique Device Identifiers (UDI), and manage clinical investigations like a pro.
Benefits You Can’t Ignore: Learn how to reduce operational costs, improve visibility with real-time reporting, and ensure traceability for compliance and audits—all with Honeywell's industry-leading expertise.
Effective Preparation Strategies: Get actionable insights on aligning your processes with EUDAMED requirements and establishing a solid project management plan for successful implementation.
Overcome Industry Challenges: Address common pain points faced by Regulatory Affairs Managers, Quality Assurance Specialists, IT Administrators, and Management Executives to safeguard your organization’s future.
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Special event information:
All participants will receive a certificate of attendance.
Date
- Sep 16 2025
Time
3:00 PM – 4:30 PM, Central European Time
9:00 AM – 10:30 AM, Eastern Time
-
00
days
-
00
hours
-
00
minutes
-
00
seconds
Speaker
-
Darrius Kilpatrick
Darrius Kilpatrick is a Product Manager at Honeywell Life Sciences, specializing in complaint handling, quality systems, and regulatory compliance for the medical device industry. With over a decade of experience, he is a subject matter expert in ISO 14971, vigilance reporting, and root cause analysis, and has worked closely with FDA and other regulatory bodies.
At Honeywell, he leads product initiatives around TrackWise and TrackWise Digital, supporting organizations in achieving EU MDR and EUDAMED compliance. Darrius has a strong background in CAPA processes and complaint investigations, and has previously held key quality roles at Medtronic and L&T Technology Services.
Partner

Honeywell
Website
https://www.spartasystems.com/Honeywell brings leading-edge quality management solutions to regulated industries. With TrackWise® and TrackWise Digital®, Honeywell provides enterprise and cloud-based QMS software solutions that help companies go to market faster and deliver the highest standards for product quality, compliance, and customer satisfaction. Honeywell is an innovator in its field, driving smart quality with first-of-its-kind AI-enabled quality solutions. By applying the latest digital technologies, our products simplify the process of quality management and guide customers toward proactive quality. The combination of Sparta Systems and Honeywell brings together Sparta Systems’ quality management leadership with over 100 years of industrial and software expertise from Honeywell. Together, Sparta and Honeywell will shape the future of digital quality and operational excellence for the life sciences industry.