Paccurate
Paccurate is the Packing Control System (PCS) for high-volume shippers. Powered by cost-aware cartonization, Paccurate helps brands, 3PLs, and distributors improve volume utilization, reduce shipping costs, and cut material waste. Our platform evaluates carrier rates, packaging constraints, and operational rules to determine the most cost-effective way to pack every order.
Shippers rely on Paccurate to run more efficient and consistent fulfillment operations, whether packing manually or through automated systems. Our goal is to ensure every order is perfectly packed.
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Runn
Runn is an innovative platform for real-time resource management that features integrated time tracking and robust forecasting abilities.
Effortlessly plan your projects and allocate resources by scheduling project phases, milestones, and time off. Switch seamlessly between monthly, quarterly, and semi-annual views to strategize for both immediate and future needs. Gain a comprehensive overview of your entire organization, allowing you to effectively manage changes in capacity, workload, and availability as you develop your plans.
Runn transforms resource management into a dynamic and visual experience through a centralized, shared interface. You can delve deeper into specific roles, teams, and tags to analyze trends and pinpoint groups that may be overbooked. Additionally, you can outline potential projects to assess how your plans could evolve as work gets confirmed.
Monitor project progress, view forecasts, and access crucial metrics with Runn, including utilization rates, project variance, and overall financial health. Utilize the platform's built-in timesheets to keep track of project advancements efficiently.
Runn also offers integrations with Harvest, WorkflowMax, and Clockify, and through its API, users can create custom integrations to connect Runn to their preferred tools, enhancing workflow and productivity even further. This versatility makes Runn a vital asset for teams looking to optimize their resource management and project planning processes.
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Deep Lens VIPER
VIPER enhances the screening process by automating the identification of remote patients at the diagnosis phase, thereby ensuring that qualified candidates are enrolled. Utilizing artificial intelligence, the system adeptly aligns patients with precision trials during a vital enrollment window, drawing on lab-agnostic genomic data, electronic medical records (EMR), and pathology data that cater to individual patient profiles and specific research demands. The specialized matching engine rigorously searches for the most appropriate clinical trials that correlate with a patient's diagnosis as soon as it is made. Moreover, VIPER integrates seamlessly into existing workflows, providing real-time notifications about patient eligibility for ongoing trials, which keeps the entire healthcare team informed during this critical period. In addition to these features, VIPER incorporates interactive dashboards that facilitate extensive data mining, enabling the collection and analysis of site and study-level patient information to effectively achieve study key performance indicators (KPIs). This holistic strategy not only boosts the efficiency of trial recruitment but also significantly aids researchers in reaching their objectives with greater success. By continuously refining its processes, VIPER stands to further revolutionize the landscape of clinical trial enrollment.
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cubeCTMS
cubeCTMS serves as a comprehensive clinical trial management platform that ensures thorough supervision of trials, which includes monitoring study sites and investigators, handling participant enrollment and visit schedules, and managing budgets and contract workflows, along with milestone reporting and document oversight. By consolidating study operations and automating key processes, it enables sponsors, CROs, and research teams to track progress in real time, coordinate activities across multiple studies, improve communication with study sites, and mitigate risks. The platform features integrated dashboards, alerts, and audit-ready documentation to maintain compliance with regulatory requirements, including readiness for FDA 21 CFR Part 11, thus empowering stakeholders to manage trial schedules, resources, and overall performance from a unified interface. Furthermore, cubeCTMS effortlessly integrates with other modules of CRScube, such as EDC, eTMF, and pharmacy/RTSM, forming a harmonious ecosystem that reduces redundancy, enhances data flow, and accommodates flexible workflows during amendments or extensive implementations. This integration not only streamlines various processes but also significantly boosts the overall effectiveness of clinical trials, ultimately proving to be an essential asset for research teams dedicated to advancing medical knowledge. With its user-friendly design and robust features, cubeCTMS sets a new standard in clinical trial management solutions.
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