Laboratory

Flatlay of chemistry lab safety rules and various glassware on a table.

How to Write an SOP That Works in the Real World

A well-run laboratory can have every compliance box checked including approved procedures, signed acknowledgments, and a complete document library. Unfortunately, this also means you can observe staff defaulting to workarounds the moment the inspector leaves. When that happens, the problem usually isn’t motivation or discipline but often the SOP itself. Most procedure documents are written

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Why Staggered Start Times May Be Your Organization’s Secret Weapon

Optimizations on the Road | Making the Most of Your Mobile Lab Operations

From 2020 onwards, largely due to Covid-19, we have seen a fundamental shift in strategy in the way we run clinical laboratories and an exponential growth in the use of mobile labs. Already used heavily for public clinics and blood donations, mobile labs have become a crucial part of the medical landscape when it comes

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Laboratory

Building a Compliance-First Mindset in High-Pressure Lab Environments

It is no exaggeration to say that clinical laboratories live under constant pressure. Whether it’s the pressure of maintaining compliance, meeting deadlines, or managing staff, there is always a race to meet turnaround times and keep operations moving. Compliance can sometimes feel like a checkbox, or worse, a burden. Regulatory compliance isn’t an annual activity.

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Close-up of a scientist examining samples under a microscope in a lab setting.

The Hidden Deficiency: Undocumented Test System Failures

Test system failures happen. It’s how your lab responds to them that determines whether you stay compliant or end up with a citation. According to CLIA and CAP, labs must document every test system failure, investigate the root cause, and implement corrective and preventive actions (CAPA). But some labs either fail to document these incidents

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