The DZS ClinPlus® suite of software covers a full range of data management and statistical procedures in clinical trials. It comprises the following:
A comprehensive SAS® based system for CRF tracking, data entry, review and coding.
This provides real time global access to ClinPlus® Data Management for data entry and review using only a browser via the internet or intranet.
This is a quick, flexible tool providing accuracy and consistency for all adverse event, drug and other coding needs.
This is a SAS® based application developed specifically for analysing and reporting data generated by clinical trials.
This is a powerful tool for creating high quality statistical tables and listings from all types of clinical data.
To place an order for the ClinPlus® suite of software, or to request a demonstration copy, please contact us.