Validated, compliant, and tailored to the way your lab actually works.
Reinvent manual workflows with automation that streamlines approvals, reduces errors, and frees the team for higher-value work. We modernize legacy systems and build secure cloud applications around your business — not a generic template.
Learn moreExperienced LIMS implementation resources for life-sciences laboratories — vendor selection, validated rollout, workflow customization, instrument integration, and ongoing optimization across CLIA, CAP, HIPAA, and 21 CFR Part 11 environments.
Learn more21 CFR Part 11 validation services covering validation plan authoring, test script creation, protocol execution, and audit defense. Staff projects with any level of expertise from Validation Consultants to QA Engineers, aligned to GAMP 5 Second Edition with CSA-compatible testing approaches.
Learn moreOur Technical Assistance Program (TAP) is designed to give you the help you have been missing when you need it! Get direct access to experts for configuration assistance, troubleshooting, or root cause analysis.
Learn moreReduce total cost of Starlims ownership from the start with an experienced partner. We provide all levels of Starlims expertise, from administrators to highly skilled developers and architects.
Learn moreSelecting the right LIMS is the most critical technology decision you will make. Our experts help you navigate the myriad of systems and select the right environment for your needs.
Learn moreWe help clients use AI as a tool that augments their team and fits inside the workflows they already have. As early adopters, we have seen the good, the bad, and the ugly of AI in production — from runaway costs to data leaks to confidently wrong outputs. We bring that experience so you capture the upside without the surprises.
Learn moreCustom clinical trial systems and integrations across CTMS, EDC, eTMF, IRT, site and subject portals, ePRO, eConsent, central-lab LIMS, safety feeds, and sponsor oversight dashboards. Twenty years of validated delivery for sponsors, CROs, and central labs, aligned to ICH E6(R3) GCP, 21 CFR Part 11, EU Annex 11, and GAMP 5 Second Edition.
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