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Electronic Case Report Form (eCRF)

The electronic capture of patient data related to a clinical trial is facilitated by an electronic case report form (eCRF). This method of information gathering replaces the paper-based systems previously used by clinical trial investigators to record and submit data related to the research and outcomes of a particular study. The switch to paperless information gathering has improved and streamlined the clinical trial data collection process in many ways. By providing a single portal in which to input data, clinical trial investigators and managers have a single source to turn to for highly organized and standardized information that can be quickly analyzed, sorted, and exported for an up-to-the minute outlook of a clinical trial’s progress.

If you are a pharmaceutical, biotech, or medical device organization about to undertake a clinical trial investigation, DDA Medical can help you securely manage, collect, and standardize data through the creation of an electronic case report form (eCRF) and database. To ensure patient data remains secure and protected, our staff of dedicated custom programmers integrate registration and login systems and store all data on a HIPAA-compliant database that is protected against outside intrusion. With years of experience in medical advertising and database development, we are sensitive to the regulations of the medical world and will work closely with each client to ensure FDA regulatory compliance. What’s more, each form will be melded around the unique requirements of each clinical study and custom administrative functionality provided to facilitate the best data management practices.  Eliminate data variation, form errors, and information mismanagement with electronic case report forms designed and developed by DDA Medical.

 

 

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