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Posts by Nichole Leahy-Glass

Get the latest updates and best practices in the MedTech industry from our blog. Join 200,000+ other MedTech professionals outperforming their peers.
Establishing a QMS
Brittani Smith
February 26, 2023

Ultimate Guide to Postmarket Surveillance of Medical Devices

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Regulatory Submission

FDA 510(k) Submission: A Step-By-Step Guide On How To Prepare Yours

Jesseca Lyons
October 4, 2022
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Post-Market Surveillance

Selecting The Ideal PMCF Activity

Jon Bergsteinsson
July 17, 2022
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About the Author

Nichole is a medical device quality and regulatory professional and a Solutions Consultant at greenlight.guru.

Product Development

How to Translate Voice of Customer into User Needs

Nichole Leahy-Glass
August 21, 2017
How well do you do at capturing “voice of customer” and translating into user needs? Read More

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