<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title>Blog | Ordo</title><description>Articles for labs working under GMP, GLP, 21 CFR Part 11 and EU GMP Annex 11: what the rules ask of AI, and how Ordo writes reports.</description><link>https://ordolabs.ai/blog/</link><item><title>How Ordo finds the deviations nobody wrote up</title><link>https://ordolabs.ai/blog/how-ordo-finds-deviations-in-a-report/</link><guid isPermaLink="true">https://ordolabs.ai/blog/how-ordo-finds-deviations-in-a-report/</guid><description>A late sample or an unplanned dilution often has no record calling it a deviation. How Ordo checks the data against the plan, and who decides.</description><pubDate>Sat, 10 Oct 2026 00:00:00 GMT</pubDate></item><item><title>Using AI under 21 CFR Part 11: what the rule actually asks</title><link>https://ordolabs.ai/blog/using-ai-under-21-cfr-part-11/</link><guid isPermaLink="true">https://ordolabs.ai/blog/using-ai-under-21-cfr-part-11/</guid><description>Part 11 never mentions AI. Here is what it does require of records an AI model touches, who signs them, and what an inspector will ask your lab to show.</description><pubDate>Sat, 10 Oct 2026 00:00:00 GMT</pubDate></item></channel></rss>