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Electronic data capture software (EDC) for clinical trials and other research studies.

Electronic Data Capture (EDC) systems are used to collect, store and manage data generated from clinical trials or other research studies in electronic forms which can either replace the traditional paper forms or be used in conjunction with paper forms for which data is then transcribed into the electronic forms. EDC systems are typically used for data collection for clinical trials but Dacima Software also specializes in data collection for other medical research study designs, including observational epidemiological study designs (cohort, case-control, and cross-sectional studies), as well as for post-marketing studies and patient registries.

EDC copy

Modern electronic data capture software applications are typically web-based and utilize a thin client. This allows end users to access the study database through the Web through a web browser without the need for the installation of an application on the local computer.

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Who uses Dacima's EDC solutions?

Our EDC software solutions are used by life sciences organizations including academic researchers, research institutions, health networks, government agencies, as well as, Clinical Research Organizations, biotechnology pharmaceutical companies.


Client Scope Dacima Software


  • Built your own databases with the user-friendly Designer module without any computer programming.
  • Shorten development and implementation time
  • Reduce costs
  • Cleaner data faster
  • Streamline data collection processes
  • Improve subject management and tracking
  • Software as a service (SaaS) or on-site installation options available
  • Manage all your studies from one application. One software application does it all. No need to purchase and manage different applications for different study designs.
  • Personalized training and support to ensure you use the software to its full potential.

Advantages of our Software

  • Flexible and configurable to meet your design, process and protocol requirements.
  • Compliant with regulatory requirements (FDA 21 CFR Part 11).
  • Complete audit trail
  • Electronic signatures and data monitoring options
  • User-friendly with data validation features and options that secure data storage
  • Comprehensive training and user guides.
  • Automatic email notification capability.
  • Integrate images for data entry through the image-based data entry features.
  • Manage database changes through the built-in workflow and versioning.
  • Standardize your data collection processes.
  • Manage patient enrollment and randomization.
  • Create a single stage or multistage subject inclusion.

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