<?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[Clearance]]></title><description><![CDATA[Audit-Ready Docs for Medical Devices]]></description><link>https://kennyposer.wixsite.com/clearance/blog</link><generator>RSS for Node</generator><lastBuildDate>Fri, 10 Jul 2026 19:39:19 GMT</lastBuildDate><atom:link href="https://www.clearance-group.net/blog-feed.xml" rel="self" type="application/rss+xml"/><item><title><![CDATA[Practical Templates for IEC 62304 Compliance Success]]></title><description><![CDATA[The medical device industry is under constant scrutiny, with regulations tightening to ensure patient safety and product efficacy. One of the most critical standards in this realm is IEC 62304, which outlines the life cycle requirements for medical device software. Achieving compliance with this standard can be daunting, but practical templates can simplify the process. This blog post will explore essential templates that can help you navigate IEC 62304 compliance successfully. Understanding...]]></description><link>https://www.clearance-group.net/post/practical-templates-for-iec-62304-compliance-success</link><guid isPermaLink="false">69baf399c22e90b51af3f703</guid><pubDate>Wed, 18 Mar 2026 18:48:57 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/21cedf_01a5fe4980de4667a7d98ef0b82aabe4~mv2.png/v1/fit/w_1000,h_576,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Kenny Poser</dc:creator></item><item><title><![CDATA[Audit-Ready Documentation for Regulated Software Projects]]></title><description><![CDATA[In the world of regulated software projects, the importance of maintaining audit-ready documentation  cannot be overstated. Whether you are developing software for healthcare, finance, or any other industry that requires strict compliance, having the right documentation in place is crucial. This blog post will guide you through the essentials of creating and maintaining documentation that meets regulatory standards, ensuring your project is always prepared for audits. Understanding the...]]></description><link>https://www.clearance-group.net/post/audit-ready-documentation-for-regulated-software-projects</link><guid isPermaLink="false">69baf38fc384c212cc96c8de</guid><pubDate>Wed, 18 Mar 2026 18:48:47 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/21cedf_f87ebaf046044f219dd36ba53a735e76~mv2.png/v1/fit/w_1000,h_576,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Kenny Poser</dc:creator></item><item><title><![CDATA[Streamline Compliance with Our Medical Device Documentation]]></title><description><![CDATA[In the fast-paced world of medical devices, compliance is not just a regulatory requirement; it is a critical component of patient safety and product efficacy. As manufacturers and developers, the challenge lies in navigating the complex landscape of documentation while ensuring that all necessary standards are met. This blog post will explore how you can streamline your compliance processes through effective medical device documentation, making your journey smoother and more efficient....]]></description><link>https://www.clearance-group.net/post/streamline-compliance-with-our-medical-device-documentation</link><guid isPermaLink="false">69baf38b392d3386b9253383</guid><pubDate>Wed, 18 Mar 2026 18:48:43 GMT</pubDate><enclosure url="https://static.wixstatic.com/media/21cedf_ae07f7f438d14b46a902f9ef8624d850~mv2.png/v1/fit/w_1000,h_576,al_c,q_80/file.png" length="0" type="image/png"/><dc:creator>Kenny Poser</dc:creator></item></channel></rss>