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

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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.
Establishing a QMS
Etienne Nichols
February 2, 2024

FDA Publishes Final Rule on QMSR

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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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Ultimate Guide to ISO 14155:2020 for Medical Devices

Jon Bergsteinsson
September 15, 2023
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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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Regulatory Submission

A Breakthrough Device that Aims to Prevent Osteoporosis

Nick Tippmann
August 18, 2021
Is your body becoming more frail? Are you worried about fractures? Do you want to improve your bone health? Osteopenia and osteoporosis are very common problems that don’t... Read More
Product Development

First-In-Class Diagnostics Tool Gets 510(k) Clearance Thanks to Greenlight Guru's QMS Software

Nick Tippmann
August 13, 2021
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Establishing a QMS

Understanding FDA's New Intended Use Rule and its Implications

Nick Tippmann
August 11, 2021
FDA published a final rule, which goes into effect the first of September, to amend its “intended use” regulations. Read More
Establishing a QMS

eQMS in Academia: Practical Learning for Biomedical Engineering Students

Nick Tippmann
July 28, 2021
Have you ever thought about the versatility of an eQMS? As it turns out, the use of one medical device eQMS solution in particular is extending across multiple sectors. Read More
Establishing a QMS

Tips for Running Better Management Reviews

Nick Tippmann
July 19, 2021
How efficient are your management reviews? Could improvements be made? It might be time to reevaluate and reconfigure your system processes to eliminate burdens and extract... Read More
Establishing a QMS

Meet a Guru: Ryan Behringer

Nick Tippmann
July 14, 2021
Guru Edge. It's what makes Greenlight Guru so unique and particularly valuable to medical device companies. These Gurus form an elite team of medical device experts who... Read More
Product Development

Navigating the MedTech Cybersecurity Ecosystem

Nick Tippmann
July 12, 2021
Cybersecurity continues to be a crucial concern for medical device safety and effectiveness in the US, for manufacturers and regulators alike. Read More
Clinical Data Collection

Managing Clinical Data Activities

Nick Tippmann
July 7, 2021
Many medical device companies experience challenges with managing clinical trials even in the most ideal settings, so what happens when big changes occur, like COVID-19 and... Read More
Establishing a QMS

Customers Rank Greenlight Guru Leader in QMS and Medical QMS Software in G2 Grid Reports for Summer 2021

Nick Tippmann
July 2, 2021
Greenlight Guru is excited to announce that we have been named a leader in G2’s Summer 2021 Grid Reports for both QMS and Medical QMS categories. Read More

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