A global and tailor-made solution to empower your trials

The CleanWEB modules can be acquired separatly. As a global solution, CleanWEB can optimize your staff productivity in an entirely certified I.S environment.

Our experts team will guide you in the computerization project of your clinical trials.



EPRO (Electronic Patient Reported Outcomes) allows patients to collect data directly from analogue scales outside of protocol visits and even from home or in real life situations.
It is natively integrated with the other modules of CleanWEB such as eCRF allowing considerable productivity gains and perfect budget control.
Available on WEB and mobile support (tablet and smartphone Android or IOS) CleanWEB ePRO innovates by allowing the video capture and audio recordings, the use of QR codes or the association with connected devices.

Clinical Trial Management System (CTMS)

This module simplifies the study’s administrative management, or the monitoring management.

Clinical Data Management System (CDMS)

This module allows the data’s check and the corrections requests, as well as medical coding with the implementation of dictionaries (MEDDRA, CIM10, etc.)

Interactive Web Responsive System (IWRS)

This module allows the use of a fully configurable online randomization (number of arms, blinding, etc.) and can be interfaced with the CleanWEB’s UT (Treatment Units)


This module allows design of electronic observation books. The Designer is a client module, installed on the user’s workstation. It allows non-IT staff (data manager, project manager, clinical research assistant) to fully configure the project’s electronic forms of the project (eCRF).

electronic Patient Reported Outcomes (ePRO)

The patient can capture or collect data directly (eQuestionnaires, analogue or digital visual scales, video or audio recordings …), outside the protocolary visits and even from the home or in real life situation. ePRO meets the need to ensure the quality of collected data.

electronic Trial Master File (eTMF)

This module allows the promoter to organize the archiving of the study’svdocuments in accordance with the regulations in force.


This module allows a panel of experts to give an opinion on a patient or event based on pre-selected data and provided anonymously in batches in read-only mode.