<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Csv-21-Cfr-Part-11 on Bioecon</title><link>https://en.bioecon.ru/technologies/csv-21-cfr-part-11/</link><description>Recent content in Csv-21-Cfr-Part-11 on Bioecon</description><generator>Hugo</generator><language>en-US</language><lastBuildDate>Mon, 06 Jul 2026 20:06:22 +0700</lastBuildDate><atom:link href="https://en.bioecon.ru/technologies/csv-21-cfr-part-11/index.xml" rel="self" type="application/rss+xml"/><item><title>Process validation and qualification (CRO)</title><link>https://en.bioecon.ru/technology/process-validation-qualification-cro/</link><pubDate>Mon, 06 Jul 2026 00:00:00 +0000</pubDate><guid>https://en.bioecon.ru/technology/process-validation-qualification-cro/</guid><description>CRO-delivered three-stage process validation and IQ/OQ/PQ qualification of biopharma equipment — media fills, cleaning validation, CSV and viral clearance under FDA/EudraLex Annex 1 cGMP.</description></item></channel></rss>