Articles about FDA Regulations, Title 21 CFR Part 11, ISO 17025, and other regulations relevant to testing laboratories.
Chain of custody programs are critical to ensuring the accuracy and reliability of your results. Read our guide to implementing a successful CoC in your lab.
From GxP regulations to ISO standards, this comprehensive guide offers everything your lab needs to master quality control and navigate regulatory compliance with confidence.
Looking to meet ISO 17025 standards in your lab? Here’s a guide to which software platforms will be the biggest help.
Looking to meet GxP standards in your lab? Here’s a guide to which software platforms will be the biggest help.
GxP outlines good practices for labs across industries. In this guide, we’ll outline how your lab can meet GxP requirements with a LIMS.
Data integrity and security are critical to the success of your lab. See how a LIMS can help protect your lab’s data.
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.
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.
Compliance with this standard helps to ensure competence, impartiality, and consistency when reporting results.
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