QBench
QBench provides a comprehensive solution for monitoring all your samples and their positions within the workflow through a unified platform. By using QBench, you can forgo the traditional reliance on spreadsheets, shared network folders, and outdated paper tracking systems. The platform enables you to review numerous PDF reports and Certificates of Analysis (COAs) before finalizing or distributing them via email. You also have the option to create customizable barcodes and labels for your samples, ensuring compatibility with standard printers and scanners. Additionally, QBench features a billing module that streamlines the creation and dispatch of invoices directly from the system. Users can access data on counts and latencies for various data types within QBench, which encompasses metrics such as turnaround times, sample counts per test, delays, and more. This innovative tool simplifies the data collection process necessary for the assays conducted in your laboratory while enhancing overall efficiency. With QBench, managing your laboratory workflow has never been more straightforward and effective.
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Lockbox LIMS
A cloud-based Laboratory Information Management System (LIMS) is designed to oversee sample tracking, test outcomes, and inventory management specifically for life sciences research, industrial quality control laboratories, and biotechnology/next-generation sequencing applications. This comprehensive system provides essential regulatory compliance support for standards such as CLIA, HIPAA, Part 11, and ISO 17025, ensuring that laboratories operate within the necessary legal frameworks. The importance of quality, security, and traceability in managing samples cannot be overstated, as these factors play a pivotal role in a lab's effectiveness and reliability. Utilizing the Lockbox LIMS platform, laboratory professionals gain the ability to meticulously oversee their samples, offering complete transparency throughout the entire process, from initial accession to long-term preservation. Additionally, LIMS analysis encompasses far more than merely tracking outcomes; the Lockbox system features advanced multilayered sample storage capabilities and location management, allowing users to customize their laboratory's storage framework with diverse options that include rooms, storage units, shelves, racks, and boxes. This flexibility empowers labs to efficiently organize and access their samples, ultimately enhancing operational productivity and accuracy.
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TruLab
Our tailored tracking solution is specifically designed for clinical trials, allowing trial managers to effortlessly download the app onto their mobile devices. With TruLab's sophisticated blockchain technology managing all intricate details, you can have peace of mind throughout the process. You no longer have to wait for samples to reach a central lab to spot potential issues; instead, you can monitor data irregularities in real-time as samples navigate through the clinical trial stages. TruLab supports continuous remote accessioning of samples, effectively tackling the notable problem that 20% of samples are either lost or rendered unusable in late-stage trials, a situation that raises ethical, logistical, and financial concerns. As the trend of collecting samples at participants' homes grows, it introduces new challenges in tracking these specimens. TruLab proficiently oversees samples no matter their location, guaranteeing their accountability from participants' residences to storage facilities, thereby bolstering the integrity of the clinical trial process. Moreover, by delivering seamless tracking functionalities, TruLab not only empowers trial managers to reduce risks but also enhances the likelihood of achieving favorable outcomes. Ultimately, this innovative solution streamlines the entire clinical trial journey, ensuring that every sample is meticulously monitored every step of the way.
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BizNet
Sarjen offers a comprehensive Clinical Trial Management System (CTMS) and Bioanalytical LIMS that brings clinical and laboratory operations together into one connected, intelligent platform. Designed to support both early-phase and late-phase studies, the solution helps sponsors, CROs, and research organizations manage the full clinical trial lifecycle with clarity and confidence. From study planning and site activation to subject tracking, financial management, and sample lifecycle oversight, every process is streamlined within a centralized environment that promotes transparency, collaboration, and control. The platform is built to drive digital transformation in clinical research by replacing fragmented systems and manual processes with automation, real-time visibility, and structured workflows. Teams can monitor study progress through intuitive dashboards, generate accurate reports with ease, and maintain regulatory compliance through standardized documentation and audit-ready data management. By unifying clinical and bioanalytical data, the system eliminates silos and enables faster, more informed decision-making across departments. As an AI-enabled solution, it enhances operational performance with predictive analytics, intelligent alerts, and automated risk identification. Features such as predictive enrollment forecasting, anomaly detection in laboratory results, smart query management, and performance analytics help reduce delays and improve overall study quality. Machine learning capabilities continuously analyze data patterns to highlight potential issues early and recommend corrective actions, allowing teams to stay proactive rather than reactive.With its flexible architecture, configurable modules, and scalable design, the platform adapts to the evolving needs of growing research organizations. By combining technology, AI, and transformation-focused innovation, it empowers clinical and laboratory teams to work smarter, accelerate development timelines.
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