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Data collection and management designed for MedTech clinical trials.

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Posts by Nick Tippmann

Get the latest updates and best practices in the MedTech industry from our blog. Join 200,000+ other MedTech professionals outperforming their peers.
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Chris Rush
April 12, 2024

Ultimate Guide to Clinical Data Management in MedTech

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Establishing a QMS

FDA Publishes Final Rule on QMSR

Etienne Nichols
February 2, 2024
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Establishing a QMS

Guide to Managing Your Medical Device on the Market and Scaling Manufacturing

Laura Maher
January 3, 2024
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About the Author

Nick Tippmann is an experienced marketing professional lauded by colleagues, peers, and medical device professionals alike for his strategic contributions to Greenlight Guru from the time of the company’s inception. Previous to Greenlight Guru, he co-founded and led a media and event production company that was later acquired.

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Product Development

Meet a Guru: Etienne Nichols

Nick Tippmann
May 24, 2021
The Guru edge: it's what makes Greenlight Guru so unique and valuable to the medical device companies it serves. Read More
Product Development

Meet a Guru: Laura Court

Nick Tippmann
May 19, 2021
What makes Greenlight Guru unique? It’s the Guru edge⁠—a team of medical device professionals with a ton of industry experience. Read More
Regulatory Submission

Regulatory Tips & Pointers from a Former FDA Reviewer

Nick Tippmann
May 17, 2021
As some veteran FDA reviewers leave and new ones are hired, knowledge is not always passed on seamlessly... Read More
Establishing a QMS

Why Demand is so High for Regulatory & Quality Jobs (and should you take advantage?)

Nick Tippmann
May 12, 2021
Great uncertainty brings great opportunities for growth...career growth. Currently, regulatory roles are one of the highest in demand in the medical device industry. Read More
Product Development

Comparing FDA’s Breakthrough Devices Program & Safer Technologies Program

Nick Tippmann
May 11, 2021
What are the differences, similarities, and potential benefits of FDA’s Breakthrough Devices Program (BDP) and Safer Technologies Program for Medical Devices (STeP)? Read More
Product Development

Why is IVDR Causing Widespread Panic throughout the Medical Device Industry?

Nick Tippmann
May 6, 2021
Is the widespread panic over the EU In-vitro Diagnostics Regulation (IVDR) justified? For many device professionals, the one year countdown to the IVDR deadline in May... Read More
Establishing a QMS

Managing Business Risk as a Medical Device Company

Nick Tippmann
May 3, 2021
It's easy to get so wrapped up in the risk management of your medical device that you forget about managing your business risk with the same level of diligence and... Read More
Establishing a QMS

Waterfall vs. Agile: Battle of the Product Development Methodologies

Nick Tippmann
April 28, 2021
Are you 'Team Waterfall' or 'Team Agile' for your product development methodology of choice? Read More
Establishing a QMS

For the Love of Internal Auditing

Nick Tippmann
April 27, 2021
Who loves internal auditing? Probably 99.99 percent of medical device professionals answered “not me!” While it may not be everyone’s favorite pastime, internal audits... Read More

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