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Greenlight Guru QMS

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

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Featured Capabilities:

Document Management Product Development Design Control Risk Solutions Training Management CAPA Management

Experience the #1 QMS software for medical device companies first-hand. Click through an interactive demo.

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SMART-TRIAL by
Greenlight Guru

Data gathering and management designed for MedTech clinical trials and operations.

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Featured Capabilities:

Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys

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Greenlight Guru Academy

Learn valuable, career-boosting skills for the Medical Device industry. Get access to hundreds of free resources as well as subscription-based courses and certifications.

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Discover the new trends, outlooks, challenges, and opportunities in the MedTech industry in 2023.

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Posts by Ryan Behringer

Get the latest updates and best practices in the MedTech industry from our blog. Join 200,000+ other MedTech professionals outperforming their peers.
Product Development
Etienne Nichols
May 11, 2023

ISO 14971 Risk Management for Medical Devices: The Definitive Guide

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Establishing a QMS

Ultimate Guide to Postmarket Surveillance of Medical Devices

Brittani Smith
February 26, 2023
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Post-Market Surveillance

Selecting The Ideal PMCF Activity

Jon Bergsteinsson
July 17, 2022
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About the Author

Ryan Behringer is a Medical Device Guru and Biomedical Engineer who prides himself on adding value in all areas of bringing a medical device to market. He has R&D, Product Development, Quality, and Sustaining Engineering experience, even utilizing Greenlight Guru to achieve 510(k) clearance, from startups to mid-sized companies. Having carried many roles in a startup environment, utilizing both Greenlight Guru and paper-based systems, Ryan understands the value in connecting the quality ecosystem. His experiences with the Greenlight Guru team as a customer led him to joining the team, where he is passionate about helping customers find the same success his team had when implementing their quality management system.

Product Development

Failure Mode Effects Analysis: What Is It & When Should You Use It?

Ryan Behringer
September 5, 2022
Failure mode effects analysis (FMEA) is one of the best-known risk management tools within engineering. Read More
Product Development

How Should Artificial Intelligence in Medical Devices be Regulated?

Ryan Behringer
September 21, 2021
Take a close look at any global industry and you’ll find them all locked in the same race toward innovation. Technology has quickened every part of every business process,... Read More
Product Development

Understanding the FDA Medical Device Classification System

Ryan Behringer
July 16, 2021
The world of medical devices is one of the most varied and complex industries around today. Innovations to research and development, data collection, and computing have all... Read More

Experience the Guru Edge

Our industry expertise extends beyond our software. Explore our other resources that are helping leading MedTech companies reach success.

Academy

Accelerate your learning and proficiency - both in Greenlight Guru solutions and industry best practices. You’ll be equipped to build key competencies for your teams.

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Community

You're not alone. We created a network of peers to connect with and learn from. At any stage of the product development lifecycle, become part of our community to accelerate your path to excellence.

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Partner Ecosystem

We have over 200 strategic partnerships with leading consultants in quality, regulatory, testing, design, and clinical.

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Resources

Do you have a unique problem that needs solving? Or maybe you’re just looking to elevate your expertise. If you're a MedTech professional looking to improve the quality of life for your patients, we have the right resources for you.

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