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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FMIS Asset Management
FMIS, which stands for Financial and Management Information Systems, is a well-established entity specializing in Asset Management solutions tailored for medium to large businesses. Renowned in both public and private sectors, FMIS empowers organizations to enhance their production efficiency through collaboration with a network of software companies, enabling smooth integration with major ERPs and CRM systems. This success stems from the combination of essential features into a cohesive solution.
Among the various software options available are Asset Budgeting, Asset Lifecycle Management, Audit Trail, Barcoding/RFID, Depreciation Management, and Inventory Tracking.
These tools represent just a fraction of the proven software solutions showcased in case studies across more than 40 countries, demonstrating their effectiveness in standardizing operational practices. Furthermore, FMIS's offerings provide a financially viable method for managing diverse organizational needs efficiently.
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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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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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