<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

SMART-TRIAL eCRF for MedTech Clinical Investigations

SMART-TRIAL eCRF is an all-in-one solution for all types of MedTech clinical investigations.  The three step Study builder enables clinical teams to create well designed and fully validated eCRF in no time.

Watch the webinar and learn about how SMART-TRIAL eCRF can improve data collection for your pre or post-market clinical investigations. 

The Optimal Choice For:
  • Pre-Market Clinical Investigations or Trials
  • PMCF Studies & Registries
  • PMPF Studies & Registries

Brought to you by SMART-TRIAL

Get your copy
Copyright 2022 SMART-TRIAL