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

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Document Management Training Management CAPA Management Audit Management Product Development

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Accelerate development with integrated design control and risk software.

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Design Controls Risk Management Risk Intelligence

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Data collection and management designed for MedTech clinical trials.

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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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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

Learning about the Real-world Impact of Design, Manufacturing, Quality & Culture on Patients

Nick Tippmann
March 24, 2021
Why is design, manufacturing, quality, and culture so important in the medical device industry? Read More
Product Development

What is the Safer Technologies Program (STeP) and Can Your Device Use It?

Nick Tippmann
March 21, 2021
What do manufacturers need to know about the Safer Technologies Program (STeP) for Medical Devices from FDA? How is STeP different from similar programs, like the... Read More
Establishing a QMS

Meet a Guru: Sara Adams

Nick Tippmann
March 18, 2021
One of the main differentiators that makes Greenlight Guru so unique is its Guru Edge. The medical device gurus ⁠are a team of medical device professionals with decades of... Read More
Regulatory Submission

Why the PMA Process is so Dreaded by Manufacturers in the US Market

Nick Tippmann
March 15, 2021
Premarket Approval (PMA) is a FDA regulatory pathway designated for Class III medical devices that has historically been known to evoke a fearful, negative response by... Read More
Product Development

Building a Startup in the MedTech Industry

Nick Tippmann
March 10, 2021
What does it take to build a successful MedTech startup? It’s a multi-million dollar question and the answer involves strong execution of a highly strategic plan. Read More
Product Development

Meet a Guru: Karen Schuyler

Nick Tippmann
March 8, 2021
What makes Greenlight Guru unique? It’s Guru edge⁠—a team of medical device professionals with a ton of industry experience. Read More
Product Development

Visualizing a Medical Device through Illustrations, Animations, and other Artwork

Nick Tippmann
March 3, 2021
Imagine using medical illustrations, animations, and other types of artwork to tell the story of a medical device, its procedures, or its manufacturer. Read More
Regulatory Submission

Everything you Need to Know about SaMD from an FDA Perspective

Nick Tippmann
March 1, 2021
Software as a Medical Device (SaMD) is a growing sector of the medical device industry. If you are interested in entering the SaMD space, what do you need to know when it... Read More
Product Development

Preparing for Remote and On-Site Inspections and Audits

Nick Tippmann
February 24, 2021
How can medical device companies be better prepared for remote and on-site inspections and audits? Practice, practice, practice so that you’re always audit-ready. Read More

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