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More than a Quality Management System: Tools for the entire MedTech Lifecycle.

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Featured Capabilities:

Document Management Training Management Product Development Design Control Risk Management CAPA Management Audit Management

Experience the #1 QMS software for medical device companies first-hand. Click through an interactive demo.

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Data collection and management designed for MedTech clinical trials.

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Featured Capabilities:

Electronic Data Capture (EDC) Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys Product Add-Ons

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Ultimate Guide to Comparing Quality Management System Solutions

This eBook compares the best QMS software solutions to help medical device companies make an informed decision when investing in a quality management system.

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FREE ON-DEMAND WEBINAR
July 17, 2024

Global UDI Updates: Navigating EUDAMED Changes & Health Authority Trends

Navigating the evolving UDI (Unique Device Identification) regulations can be challenging, but staying ahead of these changes is crucial for compliance and market access. 

Join us for an insightful webinar covering the latest updates in the global UDI landscape. This free webinar will focus on significant updates, including the EUDAMED amendments and the current status of Australia’s AusUDID, in addition to trends from other health authorities around the world.

Participants will learn a practical approach to UDI strategy for product data submissions to EUDAMED, and other best practices to streamline regulatory processes for compliance.

Specifically, This webinar will cover:
  • EUDAMED Amendment Overview: Learn about the newly adopted EU amendment and its impact on the EUDAMED timeline, including the accelerated mandatory use of specific modules by Q4/2025.
  • Post-EU MDR Strategies: Get practical advice on how to navigate the post-MDR landscape and plan your next steps effectively.
  • Australia AusUDID Updates: Stay informed about the latest developments in Australia's UDI database and what it means for your submissions.
  • Global Health Authority Highlights: Discover key updates from other global health authorities to ensure your products meet international compliance standards.

Watch the webinar
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Who should attend?
  • Quality Professionals and Management
  • Regulatory Affairs Professionals and Management
  • Medical Device Executives
Register Now  

Hosted by

Vernon Baker
Moderator:
Vernon Baker

Senior Medical Device Guru,
Greenlight Guru
John Lorenc
Presenter:
John Lorenc

Director Product Management, Life Sciences,
LexisNexis Reed Tech

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About Greenlight Guru

Greenlight Guru is the leading cloud-based platform purpose-built for MedTech companies. The end-to-end solution goes beyond traditional QMS needs by integrating cross-functional teams, processes, and data throughout the entire product lifecycle so device makers can proactively overcome execution gaps, streamline compliance, and accelerate market success.

Greenlight Guru’s platform is used by organizations across the globe that are replacing their disjointed, legacy tools and solutions to bring life-changing products to people faster, and with less risk.

Visit our homepage to learn more.

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About LexisNexis Reed Tech

Reed Tech serves almost half of the world’s top thirty medical device manufacturers, ranked by revenue. With experience ranging from start-up manufacturers to mid-size and industry-leading manufacturers, Reed Tech understands the challenges and serves the call for that ‘last mile of support’ for compliance.

They offer solutions and regulatory compliance services that help facilitate the research, collection, analysis, transformation, and submission of regulatory data to Health Authorities (US FDA, EU EUDAMED, China NMPA, Australia AusUDID and others.)

Visit their website to learn more.

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