Articles about FDA Regulations, Title 21 CFR Part 11, ISO 17025, and other regulations relevant to testing laboratories.
GxP outlines good practices for labs across industries. In this guide, we’ll outline how your lab can meet GxP requirements with a LIMS.
April 16, 2024
Data integrity and security are critical to the success of your lab. See how a LIMS can help protect your lab’s data.
April 9, 2024
ISO/IEC 17025 is a key standard for labs to meet if they wish to show the accuracy and reliability of their results. Learn what ISO 17025 is, its requirements, and how a LIMS will help your lab meet it.
March 12, 2024
FDA Title 21 CFR Part 11 is a set of regulations established by the FDA that outlines the requirements for electronic records and electronic signatures.
March 7, 2024
Compliance with this standard helps to ensure competence, impartiality, and consistency when reporting results.
September 26, 2018
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