There is a distinction baked into ISO/IEC 17025:2017 that many laboratories read past during implementation and then pay for during
They appear on the same audit checklist. They both involve standards and reference materials. In some laboratories, the same analyst
For most laboratories operating in the United States, the phrase “sample retention policy” summons an SOP binder, a storage room
A mislabeled sample is not a paperwork problem. It is a patient safety event, a regulatory citation, and — depending
Mention GLP and GMP in the same sentence to anyone working in a U.S. pharmaceutical contract lab, and you’ll get
The compliance landscape for FDA-regulated laboratories is not a monolith. It’s a patchwork of overlapping citations- and knowing which regulation
Fires don’t send calendar invites. Neither do floods, power surges, or HVAC failures. Yet most regulated laboratories are far better
When a batch of drug product fails stability testing at the 12-month mark, the first question regulators ask isn’t about
When you inspect any food and beverage QA lab during a production run and you’ll see some version of the
Most laboratories that delay adopting a Lab Information Management System cite one reason above all others: fear of disruption. Here is why
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