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 / eCOA
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.
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.