eClinical Solutions
We meet your demands across clinical operations, clinical data management and patient centricity with a suite of applications designed and supported by industry veterans.
Dacima is purpose-built to be a highly flexible and powerful Electronic Data Capture (EDC) platform. It is tailored for the design and management of clinical trials, observational studies, patient registries, clinical databases, electronic Patient-Reported Outcomes (ePRO), eDiaries, and eConsent. Founded by experts in epidemiology, medical research, and information technology, Dacima delivers advanced eClinical capabilities that meet the complex regulatory and operational requirements of modern clinical research.
Dacima is primarily used in the United States and Canada by contract research organisations, biotechnology companies, academic research groups, and non-governmental organisations.
Clindex eliminates the risk and cost of having to integrate multiple systems together by offering a fully unified platform that brings EDC, CTMS, and eTMF together in a platform that is natively integrated, not stitched together. Designed to streamline every stage of your clinical study, Clindex enables real-time collaboration, centralizes your data, and adapts to your trial’s evolving complexity. Whether you’re running a single-site study or a global, multi-center trial, Clindex delivers unmatched flexibility and cost-efficiency in one secure, regulatory-compliant system.
Clindex is primarily used in the United States by organisations operating in medical devices, diagnostics, biotechnology, imaging core laboratories, contract research organisations, and Phase I units.
Host all EDC, CTMS and eTMF data from multiple studies in one system. Manage your entire study in one inherently integrated system without the need to manage multiple vendors.
All modules are contained within a single database with a single sign-on. No need for custom APIs thereby eliminating points of failure.
Optimize your budget with streamlined workflows that reduce operational costs from the start, ensuring robust studies without compromising on quality or efficiency.
Customizable dashboards enable you to monitor study progress, identify bottlenecks, and generate insightful reports effortlessly from your EDC, CTMS and eTMF.
Eliminate uncontrolled excel spreadsheets by creating your own administrative forms and trackers.
Managing site feasibility with Clindex, eliminates manual tracking and results in the creation of a physician database which can be used for future studies.
Carenity is a patient engagement and real-world evidence platform supporting pharmaceutical and life sciences organizations with direct access to patient communities and patient-reported data. The platform enables compliant, patient-centric research to better understand patient experiences, treatment pathways, and unmet needs across a wide range of diseases.
Carenity works with pharmaceutical, biotechnology, medical device, and medtech organisations, as well as academic groups, patient advocacy organisations, CROs, and consulting firms. The platform uses real-world patient insights to support decision-making across clinical development, market access and HEOR, RWE, Medical Affairs, and commercial activities.
Our solutions are web-based and delivered through a subscription service model. They are available in both private and public cloud environments, with hosting provided in Europe or the United States according to regulatory and operational requirements.
Platform availability is supported by automated system monitoring, 24/7 technical coverage, and regularly tested business continuity procedures. Professional support and service requests are available around the clock via hotline, email, and the support portal.
