<?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[RegStalk]]></title><description><![CDATA[Regstalk provides specialized training on medical device regulations  for regulatory affairs professionals. ]]></description><link>https://www.regstalk.com/blog</link><generator>RSS for Node</generator><lastBuildDate>Tue, 02 Jun 2026 22:44:11 GMT</lastBuildDate><atom:link href="https://www.regstalk.com/blog-feed.xml" rel="self" type="application/rss+xml"/><item><title><![CDATA[EUDAMED’s First Four Modules Are Now Mandatory]]></title><description><![CDATA[What Regulatory Teams Need to Know As of 28 May 2026, the first four modules of EUDAMED are mandatory to use, marking an important step in the European Union’s move toward a more digital and transparent medical device regulatory system. This change follows the European Commission’s Decision (EU) 2025/2371, which confirmed that the modules met their functional specifications and triggered a six-month transition period. EUDAMED, the European Database on Medical Devices, is designed to support...]]></description><link>https://www.regstalk.com/post/eudamed-s-first-four-modules-are-now-mandatory</link><guid isPermaLink="false">6a1f0b36345fdf6c424e871c</guid><pubDate>Tue, 02 Jun 2026 16:59:31 GMT</pubDate><dc:creator></dc:creator></item></channel></rss>