Document and Record Control in ISO-Compliant Labs: Where LIMS Fits In
There is a distinction baked into ISO/IEC 17025:2017 that many laboratories read past during implementation and then pay for during […]
Difference Between Calibration and Quality Control in a Laboratory
They appear on the same audit checklist. They both involve standards and reference materials. In some laboratories, the same analyst
Sample Retention and Disposal Policies in the United States
For most laboratories operating in the United States, the phrase “sample retention policy” summons an SOP binder, a storage room
Sample Labeling and Traceability Standards in the U.S.
A mislabeled sample is not a paperwork problem. It is a patient safety event, a regulatory citation, and — depending
GLP and GMP Compliance for Sample Management in the USA
Mention GLP and GMP in the same sentence to anyone working in a U.S. pharmaceutical contract lab, and you’ll get