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

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Featured Capabilities:

Document Management Training Management Product Development Design Control Risk Management CAPA Management Audit Management

Experience the #1 QMS software for medical device companies first-hand. Click through an interactive demo.

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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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Ultimate Guide to Comparing Quality Management System Solutions

This eBook compares the best QMS software solutions to help medical device companies make an informed decision when investing in a quality management system.

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Electronic Case Report Forms for Medical Devices

Customizable eCRF Designed for Modern Clinical Trial Needs

Take your clinical data collection to the next level with an eCRF engineered specifically for MedTech. Design effective eCRFs that fit the needs of your clinical study and ensure high-quality data.

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1,000+ of the world's leading MedTech companies trust Greenlight Guru.

High-Quality Data Capture for Clinical Investigations

Paper-based solutions and general-purpose clinical data collection systems are costly and clunky, slowing you down, and hindering your best work. Our modern eCRF is built for the unique needs of your device, and empowers you to start your clinical data collection the right way. Get started in no time and ensure peace of mind with our pre-validated software, regulatory templates, and user-friendly study builder. 

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eCRF Made for MedTech
Clinical Needs

Improve your Medical Device clinical data collection with purpose-built features designed for capturing high-quality data faster, and more efficiently.

Standardize Your Data Collection Activities

Greenlight Guru Clinical eCRF includes 17 different ready-to-use, pre-validated question types. Use these to standardize your data collection and avoid spending time validating your question design.
Build and Scale Studies Efficiently

Build advanced eCRFs in minutes with our best-in-class study builder. Clone, reuse, and improve existing forms to streamline your study design and avoid setting up the same eCRFs again and again. 
Simplify Clinical Data Compliance

Make clinical data compliance easy with built-in GCP compliant data monitoring and validation, regulatory compliance templates, and ISO 14155:2020 pre-validation.
See Your Data Your Way

Stay on top of your clinical trial progress at all times with real-time data monitoring and all your clinical data in one place or plugged into other business systems with best-in-class API access.

Take Your Device Safety and Performance Validation to the Next Level

Purpose-built to optimize and scale medical device clinical data collection

Validation & Show Rules

Set up advanced data validation rules and question visibility based on previous data inputs.

Automatic Module Triggers

Set up automatic references to other study modules such as Unscheduled Events, Adverse Events or Concomitant Medications and create new entries directly from the eCRF.

MedTech Specific Randomization Module

User-friendly randomization module specifically designed for randomization needs in medical device clinical trials.

Integrated Adverse Events Module

The only ISO 14155:2020 & MDR Compliant AE Module fully integrated in the eCRF. AE/SAE reporting module makes it easy for MedTech teams to document, categorize, and report on AEs, SAEs in clinical investigations.

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Get a deep dive into our eCRF software and see how it can drastically change the way you collect clinical data.

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500 +

MedTech Clinical Trials

Study Setup in 2-3

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