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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.
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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featured

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.

Product Development

Case Study: How a Partnership with Greenlight Guru is Making This Dental Device Manufacturer Smile

Nick Tippmann
September 28, 2021
{% video_player "embed_player" overrideable=False, type='scriptV4', hide_playlist=True, viral_sharing=False, embed_button=False, autoplay=False, hidden_controls=False,... Read More
Establishing a QMS

Greenlight Guru Opens New Global Headquarters in Downtown Indianapolis

Nick Tippmann
September 23, 2021
Fast-growing software company to host grand opening event to celebrate company’s investment in growth in Indianapolis tech community Read More
Regulatory Submission

Past, Present, Future State (and World) of Quality in the Medical Device Industry

Nick Tippmann
September 22, 2021
Quality is a concept that is often overcomplicated in the medical device industry. With complexity comes mistakes, which is why it's so important for manufacturers to simplify Read More
Establishing a QMS

True Quality: Greenlight Guru consistently ranked the #1 QMS by users for three years in a row

Nick Tippmann
September 16, 2021
Greenlight Guru is proud to announce that for three years straight, we have been named the leader in G2’s Quality Management (QMS) category, following the recent release of... Read More
Establishing a QMS

Focusing on the Intent of the UDI Requirements from FDA's Final Guidance Doc

Nick Tippmann
September 15, 2021
When the Unique Device Identification (UDI) system was first announced by FDA several years ago, the accompanying draft guidance left much ambiguity and confusion among... Read More
Regulatory Submission

Addressing the 'Who, What, When' of Quality in the Medical Device Industry

Nick Tippmann
September 8, 2021
There are many schools of thought when it comes to the 'who, what, and when' of quality management for medical devices. Read More
Regulatory Submission

Meet a Guru: Maryann Mitchell

Nick Tippmann
September 1, 2021
What makes Greenlight Guru unique and sets it apart from other medical device solutions? It’s Guru edge⁠—a team of medical device professionals with a ton of industry... Read More
Regulatory Submission

Why Storytelling Matters for Medical Device Companies

Nick Tippmann
August 25, 2021
Medical device companies need to tell slightly different versions of their stories depending on the intended audience—investors, suppliers, regulators, clinicians, and... Read More
Establishing a QMS

CEO of High-Growth Software Company Places Top 10 in the World in Elite Rowing Competition

Nick Tippmann
August 24, 2021
David DeRam, CEO of Greenlight Guru, credits mindset techniques such as autohypnosis for both rowing and business success Read More

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