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Data collection and management designed for MedTech clinical trials.

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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

Similarities & Differences between In Vitro Diagnostic (IVD) Devices & Medical Devices

Nick Tippmann
April 21, 2021
What are the similarities and differences between an in vitro diagnostic (IVD) device machine and a medical device? Read More
Product Development

Knowing vs. Doing as Medical Device Professionals

Nick Tippmann
April 19, 2021
For medical device professionals, there are the “knowers” and the “doers.” Read More
Regulatory Submission

Greenlight Guru Named Premier QMS Software for NIH RADx Initiative

Nick Tippmann
April 15, 2021
MDQMS leader to support national COVID-19 diagnostics program through purpose-built solutions. Read More
Product Development

Pivoting Operations to Meet PPE Demand during Pandemic

Nick Tippmann
April 14, 2021
Are you on the frontlines of developing new medical devices and technologies during COVID-19? Or, are you a customer who has benefited from using them? Read More
Product Development

Pros & Cons of Being a Physician turned MedTech Inventor

Nick Tippmann
April 13, 2021
Do you fear needles and the associated pain? No one understands this fear more than physicians who see it firsthand with their patients day in and day out. And one... Read More
Product Development

3 Systems of Risk for Medical Devices from FDA

Nick Tippmann
April 7, 2021
Why does FDA have three systems in place to address and handle risk for medical devices? Each system serves a different purpose, but are all three actually necessary? Read More
Product Development

Quality Management for IVD Devices vs Medical Devices

Nick Tippmann
April 5, 2021
How are in vitro diagnostic (IVD) devices similar and different from medical devices? How should IVD manufacturers approach quality management and other key elements... Read More
Establishing a QMS

Understanding the Investigational Device Exemption (IDE) Process

Nick Tippmann
March 31, 2021
Does your medical device qualify for an investigational device exemption (IDE)? What does this process involve and what does FDA expect of these manufacturers? There... Read More
Post-Market Surveillance

Evaluating, Monitoring & Selecting Suppliers in the Medical Device Industry

Nick Tippmann
March 29, 2021
Are you a medical device professional or company seeking suppliers? Or, are you a supplier yourself? There’s a supplier management solution that will make your job a... Read More

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