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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Rave CTMS
Research teams are increasingly pressured to deliver improved results despite constraints in resources. The advancement of a clinical trial can be greatly obstructed by challenges such as uncoordinated systems, the need for manual data entry, repetitive processes, and scattered information. Therefore, it is crucial to implement a clinical trial management system that effectively integrates and streamlines workflows while providing full transparency; Medidata presents an ideal solution for this need. Rave CTMS is distinguished as the only data-centric platform crafted for efficient and intelligent management of the entire trial process. As an integral part of the Medidata Rave Clinical CloudTM, it includes all the essential features expected from a leading CTMS, along with additional functionalities. With Rave CTMS, your study teams gain the capability to plan and execute all clinical trials in a consistent and unified manner, standardizing activity planning and management at study, country, and site levels. This system facilitates the organization of study/site team creation and activation, tracks patient enrollment and milestones, monitors site performance, and addresses challenges effectively. Furthermore, Rave CTMS fosters improved collaboration and communication among team members, ultimately contributing to more successful trial outcomes, and ensuring that every aspect of the trial is managed with precision and clarity.
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Oracle Clinical One
Clinical One RTSM offers a versatile range of randomization techniques suited for both simple and complex studies, eliminating the need for programming or coding, which shortens user acceptance testing times. With the ability to self-configure your study, you can create and launch it in a matter of days instead of weeks, significantly speeding up the process. You also have the capability to monitor drug inventory levels and make instantaneous changes independently of the vendor, which helps in cutting costs associated with unnecessary change requests. By facilitating rapid adjustments, you can further reduce expenses linked to change requests and avoid delays, allowing for almost immediate study launches. This platform uniquely integrates people, processes, and data, which is crucial for enhancing the effectiveness and efficiency of clinical trials. Additionally, the incorporation of virtual elements within clinical trials not only fosters greater patient involvement but also improves the overall quality of the trial data collected. To remain competitive in the fast-paced clinical research arena, it is imperative to embrace innovative digital strategies that support quicker study start-ups, synchronize data from multiple sources, and streamline workflows. Such improvements are essential for the successful delivery of contemporary clinical research projects and ultimately contribute to advancing healthcare outcomes.
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