<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0"><channel><title><![CDATA[ClinIQ Academy]]></title><description><![CDATA[ClinIQ Academy]]></description><link>https://www.cliniq.academy/cliniq-compliance-corner</link><generator>RSS for Node</generator><lastBuildDate>Tue, 05 May 2026 09:31:54 GMT</lastBuildDate><atom:link href="https://www.cliniq.academy/blog-feed.xml" rel="self" type="application/rss+xml"/><item><title><![CDATA[ISO 14155:2026 Is Here — What Changed and What It Means for Your Medical Device Trial]]></title><description><![CDATA[ClinIQ's Compliance Corner | May 2026 If you work in medical device clinical research, whether as a sponsor, CRO, monitor, investigator, or site coordinator, ISO 14155 is the international standard that shapes how your clinical investigation should be designed, conducted, and reported. The 2026 edition is now published, and it brings meaningful updates that touch everything from how you define your research question to how you classify adverse events and oversee data quality. This post walks...]]></description><link>https://www.cliniq.academy/post/iso-14155-2026-what-changed-and-what-it-means-for-your-medical-device-trial</link><guid isPermaLink="false">69f518b590b4365cb8610aec</guid><pubDate>Sat, 02 May 2026 16:29:41 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/e8e437_873923fd75444f7e8b1dce9dffc302e8~mv2.png/v1/fit/w_1000,h_1000,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Emily Drake</dc:creator></item></channel></rss>