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About the Author

Nick Tippmann is the Chief Marketing Officer for Greenlight Guru, a MedTech Lifecycle Excellence Platform (MLE) that provides an industry-specific solution to help medical technology innovators around the world use quality as an accelerator to move beyond baseline compliance and achieve True Quality. Tippmann is 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.

Quality Management System (QMS)

Customers Rank Greenlight Guru As Leading QMS Software on G2 For 13th Consecutive Quarter

December 16, 2021
Greenlight Guru is proud to announce that it has been selected - by users - as the leading QMS for the thirteenth consecutive quarter in G2’s Winter 2022 QMS Grid Report. Read More
Product Development

How Augmented Reality (AR) is Revolutionizing Healthcare

December 8, 2021
Technology can accelerate the transformation of healthcare to improve health, quality of life, safety, and security. Augmented reality (AR) is finding its way into the... Read More
Product Development

Why FDA is Prioritizing Clinical Decision Support Software & Why You Should Care

December 1, 2021
At the top of the FDA’s agenda for the next 12 months is clinical decision support (CDS) software — what is it, why now, and why should those in the medical device and... Read More
Product Development

Why Usability Matters

November 24, 2021
Usability is essential. If you design something, anything used by humans, it needs to be designed for the users. This is especially true for medical devices. Read More
Product Development

A Special Glimpse into Medtronic's Recent Developments in Spine & Biologics Technology

November 17, 2021
Do you want to alleviate pain, restore health, and extend patients’ lifespan? Accelerate the transformation of the spine industry by making outcomes and technologies... Read More
Medical Device Industry

Greenlight Guru Launches Guru Assist, On-Demand Lifeline to Medical Device Experts

November 17, 2021
New on-demand assistance functionality offers a flexible way to leverage expert medical device support Read More
FDA Regulations

What are the Top Compliance Issues Plaguing Medical Device Manufacturers?

November 10, 2021
Medical device companies must comply with a list of strict requirements throughout the duration of their product's lifecycle. These compliance efforts will be put to... Read More
Medical Device Industry

Greenlight Guru and Formlabs Partner to Mitigate Risk and Accelerate Product Development in order to Improve Patient Outcomes

November 9, 2021
Customers benefit from leveraging industry medical specific eQMS and 3D printing Read More
FDA Regulations

Setting the Record Straight on Usability & Human Factors

November 3, 2021
What is usability? Human factors? Are they one and the same or different in the medical device industry? When do each apply? Whatever you call it, both are very... Read More

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