BEYOND DATA CAPTURE

EvidentIQ’s EDC – Our all-in-one eClinical software platform with impressive universal capabilities.
It is easy to set up and users praise its usability and multiple integrated features.
CLINICAL DATA MANAGEMENT

MEET MARVIN EDC

As of today, more than 1,300 studies worldwide have been managed using EvidentIQ EDC Software Marvin. Marvin is one of the most comprehensive eClinical solutions on the market.

Marvin provides solutions for pharmaceuticals, biotech, medical devices, cosmetics, and consumer health trials. It is easy to set up and users praise its usability and multiple integrated features.

FEATURES

FLEXIBLE FOR ANY TYPE OF STUDY

Easy Study Set-up and Management

Enjoy a well-built and flexible modern EDC application to safely collect your clinical data. A versatile software that enables easy study set-up and management. Both customers and end users value the simplicity combined with complex, customizable work flows. The integrated solution comprised of various eClinical modules, optimally supports clinical trial processes and enables seamless data flow.

BUILT FOR GLOBAL BUSINESS

Impressive Universal Capabilities

Most Clinical Trials are conducted internationally, spanning multiple countries or even continents. Marvin was designed with a comprehensive vision of the challenges global studies bring. Beginning with a centralized database that is accessible from any web browser, the addition of not just multi-language, but every language became a standard offering. Sensitive to the fact that not all regions have internet access, Marvin allows for Double Data Entry (DDE) and hybrid studies

STRONG INTERFACING

Beyond Data Capture

  • Quick and easy implementation of mid study changes
  • Advanced query management
  • Flexible for any type of study
  • Complete Audit Trail
  • (S)AE Notifications
  • Electronic Signatures
eCRF DESIGN

Composer

With EvidentIQ’s Composer, you can produce eCRF designs, document links, SDTM Tabulation and more to live in a single intuitive interface for your team. Never again struggle with any traditional office tool. The tool includes an SDTM reviewer as perfect add-on to visualize your SDTM data.

  • Smart metadata library functionality
  • Easy setup and management of amendments
  • Automatic output of the annoted CRF, data validation plan and more
  • Ensures compliance with the international CDISC ODM standard
BENEFITS

DESIGNED FROM THE GROUND UP WITH
ITS END USERS’ NEEDS IN MIND

Cleaner Data

Marvin EDC is especially great for enforcing data quality requirements. Edit checks and verifying sources are programmed into the system, ensuring that all data meets specific formats, falls within certain ranges, or has another required aspect before it’s accepted into the system.

A Unified and Comprehensive Platform

Marvin EDC delivers sponsors and CROs a cost-effective way to capture, manage and report clinical research data regardless of trial phase and complexity. Integrate multiple modules into one single user experience. Combine disparate systems into a single unified database eliminating the need for costly integrations and reconciliation.

Extensive Process Automation Features

Our Marvin EDC system can offer guidance as you take patients through a series of study events, making sure they only need the information related to their circumstances at the time. With Marvin EDC you can clarify data discrepancies or even eliminate them altogether – and can help reduce the number of in-person site visits required during a trial.

Fast Database Set-Up

With over 50 years of combined experience in the clinical trial industry, we’ve seen it all! With the help of Marvin EDC, you can reduce your database lock delays by leveraging direct input validation, edit checks and automations to capture only clean study data.
“90% of our customers chose Marvin either for its usability or quick set-up.”
Rupert Sedlmayr
Quality Manager
RESOURCES

Interview – eCRF design a pillar for clinical trials

I'm Sabine Birkner, Outbound Marketing Manager at EvidentIQ and I recently met with Kalaivani Durai, Project Data Manager at XClinical, part of the EvidentIQ Group.  Data is the linchpin for ...

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The MedDRA and WHODrug Dictionaries: What Are They and How Are They Used?

Using medical dictionaries to code clinical trial data is a key way to ensure that your clinical ...

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Meet EVIDENTIQ at the Annual SCOPE Summit of Clinical OPS Executives in Barcelona, ...

Are you going to the SCOPE Summit for Clinical Ops Executives? So are we! The 4th Annual ...

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Interview – eCRF design a pillar for clinical trials

I'm Sabine Birkner, Outbound Marketing Manager at EvidentIQ and I recently met with Kalaivani Durai, Project Data Manager at XClinical, ...

Learn More

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