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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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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

How New Training Partnership is Advancing Medical Device Knowledge & Professional Development

Nick Tippmann
June 16, 2021
Hungry for medical device industry knowledge? Greenlight Guru has you covered — now, medical device professionals can enjoy additional, sought-after training courses in the... Read More
Establishing a QMS

Greenlight Guru Announces Medical Device HQ Partnership

Nick Tippmann
June 16, 2021
New partnership with training experts will allow the medical device industry’s leading software platform to provide extended value to learners by offering additional courses Read More
Product Development

Top 3 Most Cited Issues in Medical Device Inspections from FDA FY2020

Nick Tippmann
June 14, 2021
Looking at data from 2020 FDA 483 Forms, what did FDA report as the most-cited issues during medical device inspections for the fiscal year of 2020? Understanding the data... Read More
Establishing a QMS

How Mindset Training Can Help Your Team Operate at Peak Performance

Nick Tippmann
June 9, 2021
Close your eyes, take a deep breath in, and imagine your team operating at peak performance, exceeding goals and each member feeling and working at their best. Now, breathe... Read More
Product Development

Examining the HHS Proposal for Premarket Notification Exemptions

Nick Tippmann
June 7, 2021
What are the pros, cons, and ramifications of the U.S. Department of Health and Human Services’ (HHS) proposal that impacts the medical device industry? Read More
Establishing a QMS

Crash Course on Greenlight Guru Academy: How Medical Device Professionals Stay Ahead

Nick Tippmann
June 2, 2021
If you love learning and want to level up your medical device industry knowledge on topics such as audits, document management, design controls, risk management, and more,... Read More
Product Development

Building your Brand as a Medical Device Professional

Nick Tippmann
May 31, 2021
Have you ever had to “sell” your brand to someone? To do this effectively, you must master the art of networking and selling whatever it is that you bring to the table. Read More
Establishing a QMS

Greenlight Guru Announces the Formation of Its New Regulatory Advisory Board

Nick Tippmann
May 27, 2021
Leading medical device QMS provider establishes Regulatory Advisory Board comprised of global regulatory experts Read More
Product Development

Understanding the Value of a Medical Device Guru

Nick Tippmann
May 26, 2021
Have you ever wondered, what does a medical device guru actually do? What role do they play within Greenlight Guru and what value do they bring medical device companies in... Read More

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