Greenlight Guru Clinical

Greenlight Guru Clinical

Greenlight Guru
+
+

Related Products

  • Elation Health
    88 Ratings
    Visit Website
  • AdvancedMD
    2 Ratings
    Visit Website
  • RXNT
    552 Ratings
    Visit Website
  • SurveyJS
    63 Ratings
    Visit Website
  • UnForm
    19 Ratings
    Visit Website
  • DoctorConnect
    85 Ratings
    Visit Website
  • Wave Browser
    52 Ratings
    Visit Website
  • Service Center
    123 Ratings
    Visit Website
  • Harmoni
    16 Ratings
    Visit Website
  • FrameworkLTC
    48 Ratings
    Visit Website

About

Our application provides a web-based interface to be used for collecting data from a variety of study types or clinical situations. With the built-in flexibility of its easy-to-use data capture methods to collect patient outcomes, data can be designed around any specialty, patient population, or research study. Improving the quality of care by tracking patient-reported outcomes and using population analytics. With a secure web-based interface, it is compatible with personal computers and tablets for data entry. Reports can be generated in real-time, allowing researchers to manage the entire process for single and multi-center studies, regardless of geographic location. DADOS Platform brings a top-notch user interface (UI) and do-it-yourself easy-to-use tools for clinicians and researchers to create programs or studies to bridge the gap between research and clinical care. Patients enjoy using DADOS because of its ease of use and availability anywhere.

About

Greenlight Guru Clinical is the only electronic data capture (EDC) system built specifically for medical device and diagnostics companies, not adapted from pharma. Designed exclusively for medtech, it combines an easy to use clinical data platform with industry leading customer service, helping teams generate reliable, compliant clinical data under FDA, EU MDR, IVDR, and ISO 14155 requirements. Get a single, validated platform for medical device studies, including: Electronic Data Collection and eCRF ePRO/eCOA (electronic patient and clinician reported outcomes) eConsent Randomization (RTSM) PMCF Surveys (post market clinical follow up) Adverse Events Reporting Open API Used by device manufacturers and medtech CROs running clinical investigations, PMCF studies, registries, and human factors testing. Every customer gets a dedicated customer success manager with real medtech experience and a validation package included with every product update.

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Platforms Supported

Windows
Mac
Linux
Cloud
On-Premises
iPhone
iPad
Android
Chromebook

Audience

Healthcare providers seeking a tool for improving the quality of care by tracking patient-reported outcome

Audience

Medical Device Manufacturers

Support

Phone Support
24/7 Live Support
Online

Support

Phone Support
24/7 Live Support
Online

API

Offers API

API

Offers API

Screenshots and Videos

Screenshots and Videos

Pricing

No information available.
Free Version
Free Trial

Pricing

No information available.
Free Version
Free Trial

Reviews/Ratings

Overall 0.0 / 5
ease 0.0 / 5
features 0.0 / 5
design 0.0 / 5
support 0.0 / 5

This software hasn't been reviewed yet. Be the first to provide a review:

Review this Software

Reviews/Ratings

Overall 4.0 / 5
ease 4.0 / 5
features 4.0 / 5
design 4.5 / 5
support 4.0 / 5

Pros & Cons from Real Users

Pros

  • Can be easily programmed by someone without experience coding or with software. Simple to implement rules and validations. Intuitive to use for sites and study staff. Non-blocking amendments is a great addition in the last year.
  • It is easy to navigate and use. Everything is clearly labelled. Always support from the data team. Queries are clearly labelled and simple to answer.

Cons

  • Can be a bit restrictive, for example cannot use calculated values in a validation rule which makes it more difficult to implement controls for inclusion and exclusion criteria. Export labels can be difficult to work with. Skipped or missing visits can cause issues. SDV is difficult to verify only part of a visit.
  • Having to double answer why you are changing an answer. Can be time consuming.

Training

Documentation
Webinars
Live Online
In Person

Training

Documentation
Webinars
Live Online
In Person

Company Information

DADOS
Canada
www.dadosproject.com

Company Information

Greenlight Guru
Founded: 2013
Denmark
www.greenlight.guru/clinical-electronic-data-capture-software

Alternatives

secuTrial

secuTrial

interActive Systems

Alternatives

Ennov EDC

Ennov EDC

Ennov
TrialKit

TrialKit

Crucial Data Solutions
Jeeva eClinical Cloud

Jeeva eClinical Cloud

Jeeva Informatics Solutions
Castor EDC

Castor EDC

Castor
Fusion eClinical Suite

Fusion eClinical Suite

Axiom Real-Time Metrics
Dotter.science

Dotter.science

KerNel Biomedical

Categories

Categories

Electronic Data Capture Features

Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Document Indexing
Forms Management
Remote Capture
Study Management

Electronic Data Capture Features

Audit Trail
CRF Tracking
Data Entry
Data Verification
Distributed Capture
Document Imaging
Document Indexing
Forms Management
Remote Capture
Study Management

Clinical Trial Management Features

21 CFR Part 11 Compliance
Document Management
Electronic Data Capture
Enrollment Management
HIPAA Compliant
Monitoring
Patient Database
Recruiting Management
Scheduling
Study Planning

Integrations

BSI CTMS
ChatGPT
Claude
Cursor
Gemini
Medidata
Oracle Clinical One
Prelude EDC
Tremendous
Veeva Vault

Integrations

BSI CTMS
ChatGPT
Claude
Cursor
Gemini
Medidata
Oracle Clinical One
Prelude EDC
Tremendous
Veeva Vault
Claim DADOS and update features and information
Claim DADOS and update features and information
Claim Greenlight Guru Clinical and update features and information
Claim Greenlight Guru Clinical and update features and information