CROMSOURCE provides traditional clinical data management solutions as well as an Electronic Data Capture (EDC) and Electronic Patient Reported Outcomes (ePRO) approach giving flexibility in data management solutions while always maintaining exacting standards for data quality and timeliness.
In addition to full-service clinical research trials, CROMSOURCE undertakes many stand alone and functionally based biometrics projects. Customers rely exclusively on our staff to manage all biometrics aspects from rapid data entry to final trial reports. Our experience allows us to make recommendation on the most efficient and cost-effective approach for your clinical research trial.
The CROMSOURCE Clinical Data Management team maintains a validated, 21 CFR part 11compliant EDC solution (Oracle® Clinical RDC) that is capable of handling single site Phase I trials as well as multinational, multilingual Phase II, Phase III and IV clinical research trials. Coupled with the extensive Oracle Clinical experience of our data managers, CROMSOURCE is ready to host your EDC trial. If you demands are less rigorous, for example you are conducting a registry, then Oracle® Clinical RDC offers a streamlined solution to ensure the data collection process is operationally efficient but also cost efficient. The CROMSOURCE Clinical Data Management team also has extended experience in working on many other data management and EDC platforms as may be preferred by our Sponsors.