Electronic Data Capture (EDC) Software for Faster Study Setup

Clinion EDC

Smart and fast study setup and clinical data management

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Automate and accelerate the setup and management
of your clinical trials across all phases

Set up studies in days,
not months

Configure studies quickly with our simple and inbuilt interface without depending on programming.

Benefit from faster, more
accurate data entry

Form rules like edit checks and conditional branching along with user friendly data entry forms empower users to enter data rapidly while ensuring accuracy.

Solutions designed for your unique needs

Clinion a complete and integrated environment for the configuration,
data capture and data management of clinical trials.

FDA 21CRF

21 CFR Part 11 Validated

EDC & Paper Studies

EDC & Paper Studies

eCRF Designer

eCRF Designer with Global Libraries

Document Repository

Document Repository

CDISC

CDISC Compliance

Medical Coding

Medical Coding & Multilingual CRFs

Discrepancy Management

Discrepancy Management

Cloud-Based SaaS – Pay per use model

Clinion Modules

Thought Exploration Solution

Integrated eCRF Designer

  • Drag n Drop eCRF Designer
  • Global Library
  • Staging & Production

Edit Checks Configuration

  • No-code edit check setup
  • Auto calculators
  • Conditional Branching

SDTM Integration

  • SDTM domains integration
  • Available during study design
  • SDTM SAS datasets extraction

Data Entry

  • On-fly edit checks
  • Notes & Attachments
  • Unscheduled & Recurring visits

Data Loader

  • Import multiple subject data
  • Run batch edit checks
  • Generate DCFs

Data Management

  • IV & SDV
  • Monitor & DM Locks
  • Site, Subject, Study locks

Medical Coding

  • Adverse & Conmed coding
  • Dictionaries & versioning
  • Auto & Interactive coding

Data Extraction

  • SAS and xls data sets
  • Ad-hoc data extraction
  • CRF book extraction

Integration with SDTM Libraries

Clinion global library is now integrated with SDTM libraries so that SDTM annotations can be mapped to CRF fields during eCRF creation. Features of SDTM integration include:

  • Global library with pre-configured CDISC annotated panels for all the 40 domains
  • Auto and Manual/Interactive mapping of CDISC annotations
  • CDISC Compliance Report
  • Extract CDISC SAS datasets
  • Extract CDISC define.xml
  • FDA 21 CFR Part 11 compliant with complete audit trail.

Clinion EDC,
The best fit for your clinical trial

Rapid Studies

Quick and Faster Studies

Self-Reliant

Doesn’t depend on programmers or other contractors

Data Accuracy

Ensure precision with real-time edit checks, skip logic, and other highlights

Real-Time Data

Adequate monitoring with real-time data

API Integration

Integrated with IWRS, CTMS, RBM and CDISC solutions

Adaptable Data Collection

Workable from multiple devices and browsers

Budget Friendly Ownership

Simple and easy to understand

SaaS

Effortless data sharing

Therapeutic Areas

Clinion is ideally suited for Phase II – Phase IV interventional and observational studies.
Clinion has been deployed for FDA, EU, Israel & Indian regulatory studies. The major
therapeutic areas covered by Clinion are:

Bring your entire study on one platform!

Find out how Clinion can help you