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Laboratories generate and rely on enormous volumes of data—sample records, experimental notes, test results, inventory logs, and compliance documentation. Yet many labs still manage this critical information with outdated tools, from pen-and-paper records to scattered spreadsheets. While these older methods may feel familiar, they introduce significant inefficiencies, errors, and compliance risks. Modern solutions like Laboratory Information Management Systems (LIMS) and…

As laboratories face increasing pressure to do more with less—less time, fewer resources, and tighter compliance standards—investing in laboratory informatics has become not just a strategic advantage, but a business imperative. From pharmaceutical labs to environmental testing facilities, the return on investment (ROI) for laboratory informatics solutions such as Laboratory Information Management Systems (LIMS), Electronic Lab Notebooks (ELNs), and integrated…

Falling behind in the lab doesn’t happen overnight. It starts with a missed result here, a bottleneck there, and slowly snowballs into inefficiencies that affect quality, compliance, and client trust. As science and technology continue to evolve, labs that rely on outdated methods risk becoming less competitive and more error-prone. Fortunately, there are clear warning signs and even clearer solutions…

Explore how today’s most innovative companies can inspire your lab to run smarter, move faster, and think bigger. The Lab as a System: Why Tech Giants Can Teach Us More Than We Think It might sound strange at first. What could a lab possibly learn from Netflix, Amazon, or Tesla? They don’t run tests or follow SOPs. But they do…

In clinical diagnostics, precision and reliability are not just important—they’re mission-critical. Laboratories that aim to lead in quality, patient safety, and regulatory compliance often seek accreditation from the College of American Pathologists (CAP). Recognized as one of the most rigorous and respected accreditation programs globally, CAP sets the benchmark for laboratory excellence. CAP accreditation goes beyond minimum regulatory requirements, offering…

Laboratories are the backbone of clinical diagnostics, influencing millions of healthcare decisions every year. In such a critical role, even small errors in testing can have serious consequences. That’s why the U.S. federal government enforces the Clinical Laboratory Improvement Amendments (CLIA), a comprehensive set of standards to ensure quality and reliability in all laboratory testing performed on human specimens. Whether…

For laboratories supporting product development, quality control, or regulatory testing in industries like pharmaceuticals, biotechnology, medical devices, and cosmetics, Good Manufacturing Practice (GMP) is not just a guideline—it’s a legal and operational imperative. GMP ensures that every product leaving your facility meets the highest standards of quality, consistency, and safety. Without it, even the most scientifically sound processes can lead…

In highly regulated industries, trust in scientific data is non-negotiable. Whether it’s a pharmaceutical company submitting results to the FDA or a chemical manufacturer preparing safety studies for regulatory review, data must be credible, reproducible, and traceable. That’s why Good Laboratory Practice (GLP) exists—establishing a global standard for the quality and integrity of non-clinical laboratory studies. For laboratories involved in…

In regulated laboratory environments, maintaining the integrity, security, and traceability of electronic records is essential—not only for operational excellence but for legal compliance. That’s where 21 CFR Part 11 comes in. Enforced by the U.S. Food and Drug Administration (FDA), this regulation defines how electronic records and electronic signatures must be managed to be considered as trustworthy and reliable as…

Protecting patient information is more than just a regulatory checkbox for laboratories—it’s a fundamental responsibility. Laboratories that manage patient data are required to comply with HIPAA (Health Insurance Portability and Accountability Act) regulations to ensure sensitive health information remains private and secure. Whether your lab performs diagnostic testing, integrates with electronic health systems, or shares results with providers, HIPAA compliance…