www.greenlight.guru Open in urlscan Pro
2606:2c40::c73c:67e1  Public Scan

Form analysis
0 forms found in the DOM

Text Content

This website stores cookies on your computer. These cookies are used to collect
information about how you interact with our website and allow us to remember
you. We use this information in order to improve and customize your browsing
experience and for analytics and metrics about our visitors both on this website
and other media. To find out more about the cookies we use, see our Privacy
Policy.

If you decline, your information won’t be tracked when you visit this website. A
single cookie will be used in your browser to remember your preference not to be
tracked.

Accept Decline
[Just Released] Elevate Decision-Making with Enhanced Clinical Data Reporting
See What's New


Careers Support Contact Sales
Products

 * QMS (Quality Management System)
 * SMART-TRIAL (Clinical Data Capture)
 * Academy


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

 * By Function
 * Executives
 * QA / RA
 * Product / R&D

 * By Initiative
 * Migrating From Paper
 * Managing and Assessing Risk
 * Preparing for Regulatory Submissions
 * Managing Product Development
 * Becoming Audit Ready
 * Managing Postmarket Quality

 * By Device Type
 * Class I–III
 * IVD
 * SaMD
 * Combo Product

 * By Stage
 * Startup
 * Small Business
 * Enterprise

Why Us

 * ROI Calculator
 * Guru Edge
 * Customer Success
 * Why Switch
 * Validation

Customers
Partners
Company

 * Our Mission
 * Careers

Resources

 * Resources
 * Blog
 * Case Studies
 * Checklists & Templates
 * eBooks & Guides
 * Glossary
 * Podcasts
 * Content Hub

 * Events
 * Webinars
 * Live & Virtual Events
 * True Quality Roadshow



Calculate Your ROI
See the Demo
See the Demo
 * Products
   * Quality Management (QMS)
   * Product Development Overview
   * Clinical Electronic Data Capture (EDC)
   * Academy
 * Solutions
   * By Function
     * Executives
     * QA / RA
     * R&D
   * By Initiative
     * Migrating From Paper
     * Preparing for Regulatory Submissions
     * Managing Product Development
     * Becoming Audit Ready
     * Managing Postmarket Quality
   * By Device Type
     * Class I—III
     * IVD
     * SaMD
     * Combo Product
   * By Stage
     * Startup
     * Small Business
     * Enterprise
 * Why Us
   * ROI Calculator
   * Guru Edge
   * Customer Success
   * Why Switch
   * Validation
 * Customers
 * Partner
 * Company
   * Our Mission
   * Careers
 * Resources
   * Resource Type
     * Blog
     * Webinars
     * Case Studies
     * Checklists & Templates
     * eBooks & Guides
     * Glossary
     * Podcasts
     * Content Hub
   * Events
     * Webinars
     * Live & Virtual Events
     * True Quality Roadshow

See the Demo


404 ERROR - WE'RE SORRY THE PAGE YOU'RE LOOKING FOR ISN'T AVAILABLE.

Please use the main menu to find what you're looking for.

 * About
   * Our Mission
   * Careers
   * Partner Ecosystem
   * Trust & Security
   * Support
   * All the Latest News
   * Contact Us
 * Product
   * Quality Management (QMS)
   * Clinical EDC Software
   * Academy
   * QMS Interactive Tour
   * API
   * Pricing
   * See a Live Demo
 * Use Cases
   * Document Management
   * Product Development
   * Design Control & DHF
   * Risk Management
   * Risk Intelligence
   * Change Management
   * Training Management
   * CAPA Management
   * Complaint Management
   * Nonconformance
   * Project Management
   * Audit Management
   * Supplier Management
   * Product Management
   * Product Change Management
   * Electronic Case Report Forms
   * Electronic Patient Reported Outcomes
   * Ad-Hoc Clinical Data Collection (Cases)
   * Post-Market Clinical Surveys
 * Resources
   * ROI Calculator
   * Blog
   * Free Industry Courses
   * Medical Device Glossary
   * Podcasts
   * Webinars
   * Events
   * Customer Stories
   * Checklists & Templates
   * eBooks & Guides
   * Thought Leadership Articles
   * G2 Crowd Report
   * FAQ
   * Sitemap
   * Resource Hub
 * By Initiative
   * Migrating from Paper
   * Managing and Assessing Risk
   * Managing Product Development
   * Becoming Audit Ready
   * Preparing for Regulatory Submissions
   * Managing Postmarket Quality
 * Top Guides
   * ISO 13485
   * ISO 14971
   * ISO 14155:2020
   * 21 CFR Part 820
   * 21 CFR Part 11
   * 510(k) Submission
   * Design Controls
   * Design Verification
   * CAPA
   * IQ, OQ, PQ
   * EDC Systems
   * eCRF



© 2023 Greenlight Guru. All rights reserved. Legal Info