EtrewoTM is an enterprise technology platform that enables biopharmaceutical teams to conduct custom-post-commercialization studies ranging in scale and shape from investigator-initiated studies and registries to multiple large-scale outcome trials (both prospective and retrospective). Cost optimization, driven by intuitive technology with the option for allied services, makes it a platform of choice for our customer teams across geographies.
Our customers have deployed EtrewoTM to generate outcomes data, insightful practice trends and/ or quality evidence to manage their products’ life cycles efficiently in their highly competitive landscapes with virtually no dependencies.
Web/cloud-based, device-friendly platform; accessible through any browser and on any device
The eCRF can be built in a very short span of time. It can easily and swiftly be configured to launch the study.
Real-time reports and 24/7 access in desired format and filters. Gives early trends and outcomes of study.
Role-based authenticated access, e.g. investigator, CRC, sponsor, data manager, etc.
eCRF data fields/questions and layout are fully configurable to meet the sponsor’s requirements, without compromising the quality of the architecture.
21 CFR part 11, HIPAA, Global Data Protection Regulations (GDPR)-complaint, fully validated with comprehensive IQ, OQ, PQ documentation.
Strong system authentication and security; hosted on AWS (Amazon web services).
Same eCRF available in different languages
Enables the product to easily integrate with external systems/applications
.Net 4.6, C#, SQL Server 2017, Angular5, HTML5, CSS3, Bootstrap4, jQuery3.3
Hosted on Amazon Web Services (AWS)
Snapshot-Based Data Backup
24/7, 99.90% uptime