A cloud LIMS that tracks samples, tests results, and manages inventory for life science research, industrial QC labs, and biotech/NGS. Includes regulatory support for CLIA and HIPAA, Part 11 and ISO 17025. The quality, security, traceability, and traceability for samples is crucial to a lab's success. Laboratory professionals can use the Lockbox LIMS system to manage their samples. They have full visibility of every step of the sample's journey from accession to long-term storage. LIMS analysis is more than just tracking results. Lockbox's multilayered sample storage and location management functionality lets you define your lab's storage structure using a variety location options: rooms and storage units, shelves and racks, boxes and boxes.
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Labs don't need another LIMS. They need a complete operating system for modern lab operations - and that's QBench, reshaping everything from order placement through sample processing to automated reporting.
Simple. Powerful. Adaptable. Where other LIMS force labs into rigid structures built on heavy custom code and vendor dependency, QBench moves with you. It bends. It adapts. Your processes evolve, and QBench evolves too.
It adapts to your secret sauce. Every lab has its own workflow, its own rhythm, and QBench respects that with unmatched configurability. You shape the workflows. You define the data fields. You stitch together the automations. QBench's former bench scientists work alongside you throughout, offering expert guidance and workflow suggestions.
It automates the tedious work. File parsers and a robust API connect QBench to the instruments and systems you already run, so data flows on its own. No manual entry. No transcription errors.
It unifies everything in one platform. Real-time inventory. A dedicated portal giving clients instant access to results. Built-in analytics. A QMS module that keeps you audit-ready, always.
QBench helps labs work smarter - cloud-based, secure, and always evolving, like the science it supports.
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Prendio For Biotech
Prendio was specifically designed for biotech, unlike other eProcurement systems. We have created a simple, efficient, and affordable procure to pay solution that increases efficiency and decreases administrative burden. This reduces research time and speeds up development. With our intuitive functionality, you can easily create and save carts for all your favorite suppliers. You can view order history and status, and get convenient notifications right from your dashboard. Browse the catalog to place orders and compare item ratings. You can also take advantage of our punchouts. To make it easy to reorder, save carts as templates. We offer comprehensive, free punchouts that are custom-made for your company. This automated purchasing solution is made possible by our industry-leading supplier network. Finance can be sure that they are only paying for goods or services that have been received by matching packing slips and invoices digitally.
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Scientist.com
Our marketplace was developed to enhance the sourcing of regulated services effectively. With COMPLi®, organizations can establish a robust compliance framework that offers leadership reassurance about the integrity of sourcing across various research domains. The platform facilitates the automatic tracking of purchases, contract management, payment processing, and the integration of spending data into accounting systems. Recognized for its excellence, our platform aids pharmaceutical companies, biotech firms, and academic institutions in procuring regulated services and materials from external vendors. Whether you're involved in research, procurement, or service provision, COMPLi® is designed to address your compliance and governance challenges. Additionally, COMPLi® alleviates the administrative workload for providers of regulated services, fostering efficient customer interactions that ultimately lower expenses and expedite scientific inquiry. By enhancing compliance and governance across diverse regulated service sectors, COMPLi® empowers organizations to focus more on innovation and less on regulatory hurdles.
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