EDC Systems for eCRF Design
Data management in clinical trials is not less important than the overall study itself. That is why following the latest trends that provide exceptional opportunities for handling the results of the clinical trials is highly important.
Over the last several years, electronic case report forms (eCRFs) have become the foundation of data management in clinical trials. Those are created in electronic data capture (EDC) systems that make it possible to organize the data in an effective manner, which makes it highly convenient for clinical trial researchers and workers.
What is an EDC system?
A typical EDC system might also be known as the eCRF software for designing clinical trial report forms. Such applications allow for creating, adjusting, and reusing forms to capture the patients’ data and clinical trial results and observations.
An EDC system is often a part of the complex software applications for medical workers and researchers. It is usually integrated with other applications that facilitate handling the overall clinical trial study and derivation of its outcomes.
An EDC system might also be compatible with other similar applications produced by other software companies. As a result, it makes it easier to share reports and results with different teams that need to evaluate the clinical trial outcomes.
Using eCRF software in clinical trials may also facilitate a range of other processes related to the overall research. Capturing data in the electronic format makes it more accessible for workers in different departments. Also, data security gets to the next level as modern mechanisms based on cryptography keep the data protected.
Design eCRF in EDC system
A major privilege of any EDC system is that it helps with eCRF design for various clinical studies. It makes it possible to craft eCRFs from scratch or create them based on the previous ones used as a template.
While creating eCRF requires considering many points for recording the data in the most comprehensive manner, EDC allows doing so. Even though it might take weeks to establish a proper EDC system, the eCRF software named ryze helps to do it much faster.
The EDC systems enable the creation of eCRFs according to the latest CDISC standards. Those are very important as compliance with CDISC standards means that the clinical trial results are actual and thus could be passed over to other medical organizations.
Another positive aspect of designing eCRFs in EDC systems is the ease of making reports and data analysis. When all the data is systemized and structured, the reports can be generated automatically. This helps to draw conclusions and general tendencies of the clinical trial study. Moreover, data analysis is done highly effectively when the EDC system is used.
One more positive aspect associated with the EDC systems is the data reuse opportunity. This means that the previously designed eCRFs for clinical trials could be adjusted and reused for newer studies. As a result, it helps researchers and medical workers to save lots of time and improve the effectiveness of the overall study.
