<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

eCRF template tool - LinkedIn Ad image

SMART-TRIAL's eCRF Template

Reduce setup errors and prepare eCRF specifications beforehand in a format that allows study teams to review and adjust accordingly.

By using a standardised template you have a structured way of documenting eCRF specifications for your EDC setup.

  • Ensure consistency between studies
  • Simplify review and QA of the eCRF specs
  • Significantly reduce EDC setup time

Get your copy
Copyright 2022 SMART-TRIAL