The end goal of any clinical trial is to obtain useful data that underscores the safety and/or efficacy of the drug, therapy, or device being assessed. To achieve this, validated processes are essential to carefully handle the data. This ensures potential issues can be identified early, and keeps data internally consistent throughout the study. 

Datapharm’s experienced staff can set up an Electronic Data Capture system for you to ensure all planned datapoints are collected. We use an efficient combination of automatic and manual methods to check the plausibility and accuracy of the entered data.

CDISC standards are becoming the industry standard for regulatory submissions. Our statisticians are familiar with CDISC formats and the necessary conversion of data, to allow the involved process in data conversion to be expedited for regulatory submission.

Part of having usable data is the ease with which it can be looked at. Datapharm is able to provide a study's database in any number of formats for analysis. In addition, user-friendly ICH-compliant data listings can be generated in pdf form for anyone to review during the study.