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A global solution for the electronic management of clinical trials
EDC – IWRS – CTMS – CDMS – ePRO – IoTs – eTMF …

CleanWEB is a secure Internet platform dedicated to managing national or international clinical electronic studies, registries and cohorts, mono or multi-centric. It is especially made for projects of all kinds: clinical trial from phase I to IV, real-life based studies, veterinary studies, epidemiological studies.

Certifications : CDISC ODMISO 9001:200821 CFR Part 11 Compliance

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A powerful, modular and inter-exploitable information system: to support the implementation, management and project monitoring, as well as the investigators’ tasks; facilitate patients’ recruitment and their compliance.

The « software + services » packs are customizable to meet everyone’s expectations.

The pack “Project”

Effectiveness and cost-efficiency.

Based on the Clinical study Protocol (and eventually on the CRF project), our “clinical operation” dedicated team is implementing the project (eCRF and data entry check function’s parameterization, validation plan’s implementation, randomization, users accounts etc.) in mutualized and readily available environment. The CleanWEB license, project management, secured hosting, software maintenance, the decommissioning, as well as the user support needed till the end of the project are included in the rental-package in a SaaS mode – Software as a Service.
– As an option : accredited HDS hosting (Health Data), connected objects, creation of a dedicated graphic layout (for ePRO module for instance), customized add-ons (integration with third party system, mini-websites for recruiting etc.)
– In partnership with CRO Alliance: monitoring coding, statistical analysis.

Pack « dedicated Cloud »

Autonomy – “Hosting” Trusted third party – Fee-for-use

You are interested in a global solution for all your clinical studies, available right away and without having to worry about hosting? You would like a usage-based pricing? Our technical service staff will create for you a dedicated environment for your clinical studies. Our “clinical operations” team will be able to offer a “skills transfers pack” in case you would like to be completely independent to manage your projects.

Pack “Full Licence”

Integral skills transfer – independence – S.I Integration Clinical research

You are interested in a solution for all you clinical studies and you already have your own hosting platform? You would like to integrate with other software from your S.I clinical research? This pack will grant you access to a license with unlimited usage. Our technical staff will deploy CleanWEB together with your team on your hosting platform and will provide you with all the documentation and processes for maintenance and supervision. In case needed, specific add-ons will be created with a view to fully integrating the tool with the other software that are part of your Information System “Clinical Research”. Our “Clinical Operations” team will provide with the skills transfer to your operational teams.

Pack “Real World Studies”

ePRO – eCOA, connected objects – Observance

You are interested in a real-life case-study with the implementation of sensors wore by the patients or installed in their homes, the deployment of auto-survey ePRO to monitor the observance or the patient’s quality of life? You are keen to use the patient’s smartphone, or a connected mobile device (smartphone, tablet) provided especially for the project? We provide you with our HUB clinical data and its secured hosting platform environment (HDS in option), as well as the whole of our connected devices. In case you would like to use the EDC-CTMS modules of CleanWEB, we already have it accredited under 21 CFR Part 11. We can also manage the integration with your EDC and CTMS system in case you already have one.

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