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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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Featured Capabilities:

Design Controls Risk Management Risk Intelligence

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Data collection and management designed for MedTech clinical trials.

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Featured Capabilities:

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 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.
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

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.

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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

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