<img src="https://ws.zoominfo.com/pixel/OJkQgdjSvoid2NFoB5Qs" width="1" height="1" style="display: none;">
Careers Support Contact Sales
Products

Greenlight Guru QMS

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

Learn More

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.

View Product Tour

SMART-TRIAL by
Greenlight Guru

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

Learn More

Featured Capabilities:

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

Get a personalized demo of SMART-TRIAL by Greenlight Guru today.

See the demo

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.

Learn More
Solutions
Why Us
Customers
Partners
Company
Resources
image-mckp (1)-1

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

Grab a copy
See the Demo
See the Demo
See the Demo
checklists and templates

7 Steps for Writing a Nonconformance Report

7 steps for writing a nonconformance report - slide-in cover

A 7 step process for writing an effective nonconformance report.

Want more free medical device resources? Click here to access our full library of downloadable content!
© 2023 Greenlight Guru. All rights reserved. Legal Info

Yes, I want the resource!
© 2023 Greenlight Guru. All rights reserved. Legal Info