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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Pensero represents an advanced platform that utilizes artificial intelligence to improve observability and performance metrics, specifically tailored for engineering teams and their leaders to achieve a more profound comprehension of software development activities. By automating the gathering and integration of "work signals" from the tools your team currently employs, such as code repositories, issue trackers, and communication apps, it converts fragmented tasks into detailed insights. These insights are then translated into objective metrics, real-time dashboards, and thorough reports that not only indicate the amount of work accomplished but also incorporate complexity and workflow nuances. Utilizing Pensero allows you to instantly access information about active projects, individual team member contributions, and the overall workflow within the organization, while also revealing how team productivity correlates with strategic initiatives and business goals. Its smooth integration and ability to scale ensure that teams can quickly turn raw data from diverse tools into actionable insights that enhance performance. By streamlining the analysis of software development processes, Pensero ultimately enables organizations to refine their development efforts more efficiently than they ever thought possible, fostering an environment of continuous improvement and innovation.
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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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CSAM Studies
CSAM Studies, previously referred to as MedSciNet Studies, is a powerful and flexible online platform that has effectively facilitated the management of clinical research for the past twenty years. This internet-based resource for medical studies offers an extensive array of applications aimed at the hosting, administration, and supervision of projects of various sizes and complexities. CSAM MedSciNet's standard offerings encompass all critical components needed to launch a fully functional study or clinical trial. Moreover, this exemplary solution is enhanced with features that support dynamic and interactive data entry forms, customizable workflow designs, and advanced tools for data validation, analysis, and exportation. By utilizing these capabilities, researchers can adopt a thorough and efficient strategy for overseeing their clinical trials. As a result, CSAM Studies continues to evolve, meeting the changing demands of medical research with innovative solutions.
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