< Back to all authors

Jodi Granger

Jodi Frasier

Director of Regulatory Affairs

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

With over 36 years of experience in regulatory and quality roles, Jodi Frasier 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

Medical Device Registration Across Global Markets

Medical Device Registration Across Global Markets: A Strategic Guide

June 17, 2026

Read Medical Device Registration Across Global Markets: A Strategic Guide

link
webinar Regdesk

Faster Global Submissions: Using Prior Approvals to Your Advantage

May 28, 2026

Read Faster Global Submissions: Using Prior Approvals to Your Advantage

link

What the FDA’s QMSR Means for Medical Device Manufacturers Right Now

April 30, 2026

Read What the FDA’s QMSR Means for Medical Device Manufacturers Right Now

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

Are You Running a Reactive Regulatory Team Without Knowing It?

February 26, 2026

Read Are You Running a Reactive Regulatory Team Without Knowing It?

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

Essential Principles of Safety and Performance: A Strategic Compliance Guide

February 18, 2026

Read Essential Principles of Safety and Performance: A Strategic Compliance Guide

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

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

February 17, 2026

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

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

EUDAMED Modules Guide: Structure, Deadlines, and Regulatory Impact

February 10, 2026

Read EUDAMED Modules Guide: Structure, Deadlines, and Regulatory Impact

link
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

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

link
# #