Time
4:00 PM – 5:30 PM, Central European Time (CET)
10:00 AM – 11:30 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. You’ll also discover the NEW TrackWise EUDAMED Management Solution.
Speaker
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Darrius KilpatrickProduct Manager at Honeywell Life SciencesDarrius 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.trackwise.com/Honeywell Life Sciences, the makers of TrackWise, is on a mission to accelerate innovation for a healthier future. From manufacturing life-saving drugs and devices to safeguarding supply chain continuity, Life Sciences organizations partner with Honeywell to solve their most critical challenges and drive meaningful patient, customer, and business outcomes.
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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.
Time
4:00 PM – 5:30 PM, Central European Time (CET)
10:00 AM – 11:30 AM, Eastern Time (ET)
Speaker
-
Darrius KilpatrickProduct Manager at Honeywell Life Sciences
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.trackwise.com/Honeywell Life Sciences, the makers of TrackWise, is on a mission to accelerate innovation for a healthier future. From manufacturing life-saving drugs and devices to safeguarding supply chain continuity, Life Sciences organizations partner with Honeywell to solve their most critical challenges and drive meaningful patient, customer, and business outcomes.
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