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Jodi Granger

Jodi Granger

Director of Regulatory Affairs

LinkedIn: https://www.linkedin.com/in/jodilynnfrasier/

With over 36 years of experience in regulatory and quality roles, Jodi Granger brings deep subject-matter expertise to RegDesk. Before joining the team, she led global regulatory teams at top medical device and IVD companies, overseeing strategy and compliance for diverse product portfolios. 

At RegDesk, Jodi advises on regulatory content, supports customer success, and ensures the platform reflects up-to-date, real-world requirements. Jodi is a respected leader in the industry and a passionate advocate for innovation in regulatory operations. Jodi prides herself on being customer focused, while developing regulatory processes that not only ensure regulatory compliance but also help establish regulatory as a partner in achieving growth for the company.

Articles by this author

key-takeaways-from-regdesks-from-manual-to-modern-webinar

Are You Running a Reactive Regulatory Team Without Knowing It?

February 26, 2026

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essential-principles-of-safety-and-performance-a-strategic-compliance-guide

Essential Principles of Safety and Performance: A Strategic Compliance Guide

February 18, 2026

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eudamed-modules-guide-structure-deadlines-and-regulatory-impact

Regulatory Information Management: Streamlining Regulatory Data, Submissions, and Compliance

February 17, 2026

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eudamed-modules-guide-structure-deadlines-and-regulatory-impact

EUDAMED Modules Guide: Structure, Deadlines, and Regulatory Impact

February 10, 2026

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eudamed-in-focus-new-modules-system-evolution-and-impact-on-medical-device-companies

The Clock Is Ticking: What Medical Device Manufacturers Need to Know About EUDAMED’s Mandatory Transition

January 29, 2026

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