Lambda-Plus
Telemedicine Technologies is a market leader in e-Health solutions, specializing in clinical research with its flagship platform, CleanWeb™, which manages clinical trials, registries, observational studies, and early access programs across more than 64 countries. The company is committed to innovation, quality, and international deployment, supporting over 20,000 investigative centers, 3 million patients, and 50,000 users worldwide. It offers a wide range of solutions including data management, AI & data visualization, training, user support, hosting, and specialized modules for clinical research and hospital management. With certifications like ISO 9001:2015, ISO 27001, and CDISC/ODM, and compliance with GDPR and FDA regulations, Telemedicine Technologies aims to improve healthcare delivery and clinical research efficiency globally.
Industries
Nr. of Employees
small (1-50)
Lambda-Plus
121 rue d’Aguesseau, 92100, Boulogne-Billancourt, France
Products
Modular eClinical platform (EDC + modular modules)
A modular electronic clinical platform offered in SaaS or project-based deployment including core modules (eCRF, ePRO, randomisation, designer, directories) and optional modules (CTMS, eTMF, eConsent, imaging, remote monitoring).
Mobile patient recruitment and site-matching application
Multi-device application that uses algorithmic matching to identify patients potentially eligible for studies in real time and increases investigator visibility of trials.
Electronic Investigator Site File (eISF)
Digital version of the paper investigator site file enabling collection and storage of essential regulatory documents in compliance with Good Clinical Practice.
Hospital patient pathway and service planning platform
Platform to computerise medical protocols and plan, standardise and monitor patient pathways across hospital departments, with workflow-driven scheduling and administrative interfacing via HL7.
Medical imaging management module
Module to manage imaging in clinical trials: upload from browser or eCRF, associate metadata variables, anonymise images automatically or semi-automatically, and provide a DICOM/video viewer.
Modular eClinical platform (EDC + modular modules)
A modular electronic clinical platform offered in SaaS or project-based deployment including core modules (eCRF, ePRO, randomisation, designer, directories) and optional modules (CTMS, eTMF, eConsent, imaging, remote monitoring).
Mobile patient recruitment and site-matching application
Multi-device application that uses algorithmic matching to identify patients potentially eligible for studies in real time and increases investigator visibility of trials.
Electronic Investigator Site File (eISF)
Digital version of the paper investigator site file enabling collection and storage of essential regulatory documents in compliance with Good Clinical Practice.
Hospital patient pathway and service planning platform
Platform to computerise medical protocols and plan, standardise and monitor patient pathways across hospital departments, with workflow-driven scheduling and administrative interfacing via HL7.
Medical imaging management module
Module to manage imaging in clinical trials: upload from browser or eCRF, associate metadata variables, anonymise images automatically or semi-automatically, and provide a DICOM/video viewer.
Services
End-to-end study data services including eCRF design, annotated CRFs, DMP/DCP, data cleaning/programming, data validation, integration, reconciliation, database lock and SDTM mapping.
Machine-learning pipelines and advanced statistics applied to aggregated clinical data to generate dashboards, automated classification and predictive analytics.
Certified training courses for platform configuration, eCRF design and end-user autonomy, delivered under a national quality certification.
Multilingual (French and English) tiered support available via web portal, hotline and remote access under SLA and contractual terms.
Health-data hosting with geographically separated primary and secondary sites, ISO-certified infrastructure, redundancy, daily backups and optional mirroring.
Digital solutions (multi-device apps and web) to facilitate patient identification and recruitment at sites through algorithmic matching and real-time detection of eligible patients.
End-to-end study data services including eCRF design, annotated CRFs, DMP/DCP, data cleaning/programming, data validation, integration, reconciliation, database lock and SDTM mapping.
Machine-learning pipelines and advanced statistics applied to aggregated clinical data to generate dashboards, automated classification and predictive analytics.
Certified training courses for platform configuration, eCRF design and end-user autonomy, delivered under a national quality certification.
Multilingual (French and English) tiered support available via web portal, hotline and remote access under SLA and contractual terms.
Health-data hosting with geographically separated primary and secondary sites, ISO-certified infrastructure, redundancy, daily backups and optional mirroring.
Digital solutions (multi-device apps and web) to facilitate patient identification and recruitment at sites through algorithmic matching and real-time detection of eligible patients.
Expertise Areas
- eClinical platform deployment (SaaS and project-based)
- Clinical data management and CDISC/SDTM standards
- Clinical trial management and monitoring (CTMS, remote monitoring)
- Medical imaging management in clinical studies (DICOM/non‑DICOM)
Key Technologies
- Electronic Data Capture (eCRF/EDC)
- ePRO / eCOA
- Electronic consent (eConsent)
- Interactive Web Response System (IWRS) / randomisation
News & Updates
Webinar on EU procurement in digital health, promoting interoperable solutions.
Representation at the Japan Health Exhibition 2025, engaging with healthcare leaders.
Discussion on AI and agility in clinical trials.
BSMA Europe Award 2024
Award received for the CleanWeb™-RTSM module, streamlining supply management for trials.
Webinar on EU procurement in digital health, promoting interoperable solutions.
Representation at the Japan Health Exhibition 2025, engaging with healthcare leaders.
Discussion on AI and agility in clinical trials.
BSMA Europe Award 2024
Award received for the CleanWeb™-RTSM module, streamlining supply management for trials.