Ennov CTMS
Ennov CTMS facilitates the end-to-end management of clinical trials. The software allows sponsors to be more efficient, to make better decisions, to ensure compliance, to select investigators well, to monitor patient recruitment and to manage finances. Ennov CTMS includes comprehensive directories to manage site personnel (investigators, sub-investigators, study coordinators, pharmacists) and organizations (hospitals, competent authorities, CROs, suppliers).
Ennov CTMS provides functions for tracking patients, patient visits, EDC data, activities, queries, deviations, adverse events, drug supply, monitoring visits and finances. A full complement of reports and dashboards provide total visibility into the status of each study, country, site and investigator to provide the information necessary to make the best decisions possible.
- Comprehensive CTMS software
- Integrated with Ennov Clinical Data Management
- Clear visibility into investigational sites
- Integrated workflow
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ValueStreamer
Streamline your shop floor management with ValueStreamer, the all-in-one digital solution. Easily view team-specific KPI boards, handle deviation management on the spot, and solve problems with binding tasks using the PDCA and A3 problem solving methods. Automatically aggregate KPIs across all hierarchies.
Effortlessly connect to your existing IT systems like MES, ERP, and EDGE through our standardized REST API. Go beyond basic BI and experience true collaboration within your company. Save time, effort, and money with ValueStreamer.
Features include:
- Target/actual key figures with automatic aggregation of KPI values
- Linking of top issues, go & see, feedback, and actions
- Deviation management with prioritization in the Pareto chart
- T-Cards for process confirmation on the shopfloor
- Connectivity via REST API to systems like MES and ERP
- Mapping of typical company processes in medium-sized businesses such as AAP, product development process, CIP, and Kanban.
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ArcheMedX Ready
Pharma and biotech trust Ready by ArcheMedX to better equip their trial teams, improve decision making, and reduce study delays. Prevent the most common sources of study delays, by better understanding which sites and teams are most prepared to start and effectively conduct the study. Reduce time and costs spent resolving issues, especially early in the trial. Confidently know which sites truly understand your patient eligibility requirements. Enjoy knowing they’ll be better equipped to enroll eligible patients sooner, hit enrollment targets, and avoid screen failures. With detail down to each individual and study objective, you can know with confidence that trial team members truly understand the specifics of the protocol. Predict where risks lie so you can prevent them, and experience fewer deviations overall.
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eAdjudication
Ethical eAdjudication is an innovative endpoint adjudication and e-clinical software solution. With an intuitive and user-friendly cloud service designed exclusively for study leaders, QA staff, and committee members, Ethical eAdjudication offers the simplest solution to seamlessly manage event database, committee assessment, and disagreement and consensus meetings in a GxP controlled environment. By leveraging Ethical eAdjudication, users are given the opportunity to accomplish independent review and adjudication procedures in an effective, timely, and quality controlled manner.
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