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    <description>Pharmaceutical compliance insights for compounding pharmacies</description>
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      <title>What the HHS Peptide Reclassification Means for Compounding Pharmacies</title>
      <link>https://complirx.io/blog/hhs-peptide-reclassification</link>
      <pubDate>Fri, 27 Feb 2026 00:00:00 GMT</pubDate>
      <guid>https://complirx.io/blog/hhs-peptide-reclassification</guid>
      <description>How the March 2025 HHS decision restored compounding pharmacy access to key peptide APIs and what compliance steps you need now.</description>
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      <title>Peptide Compounding Compliance Checklist</title>
      <link>https://complirx.io/blog/peptide-compliance-checklist</link>
      <pubDate>Wed, 05 Mar 2026 00:00:00 GMT</pubDate>
      <guid>https://complirx.io/blog/peptide-compliance-checklist</guid>
      <description>A comprehensive compliance checklist covering supplier qualification, documentation, potency testing, stability, and adverse event monitoring.</description>
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      <title>503A vs 503B: Choosing the Right Peptide Compliance Path</title>
      <link>https://complirx.io/blog/503a-vs-503b-peptide-compliance</link>
      <pubDate>Tue, 11 Mar 2026 00:00:00 GMT</pubDate>
      <guid>https://complirx.io/blog/503a-vs-503b-peptide-compliance</guid>
      <description>A detailed comparison of 503A and 503B peptide compliance requirements to help pharmacies choose the right path.</description>
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      <title>5 Environmental Monitoring Mistakes That Fail FDA Inspections</title>
      <link>https://complirx.io/blog/environmental-monitoring-mistakes-fda-inspections</link>
      <pubDate>Wed, 18 Mar 2026 00:00:00 GMT</pubDate>
      <guid>https://complirx.io/blog/environmental-monitoring-mistakes-fda-inspections</guid>
      <description>Environmental monitoring failures are among the most common FDA inspection findings. Learn the five critical mistakes that lead to 483 observations and how to avoid them.</description>
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      <title>21 CFR Part 11 Compliance Checklist for Compounding Pharmacies</title>
      <link>https://complirx.io/blog/21-cfr-part-11-compliance-checklist</link>
      <pubDate>Fri, 20 Mar 2026 00:00:00 GMT</pubDate>
      <guid>https://complirx.io/blog/21-cfr-part-11-compliance-checklist</guid>
      <description>A practical checklist covering the key 21 CFR Part 11 requirements for electronic records and signatures in compounding pharmacy operations.</description>
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      <title>How to Build a USP 797 Training Program That Actually Works</title>
      <link>https://complirx.io/blog/usp-797-training-program</link>
      <pubDate>Sun, 22 Mar 2026 00:00:00 GMT</pubDate>
      <guid>https://complirx.io/blog/usp-797-training-program</guid>
      <description>A practical guide to building and maintaining a USP 797 training program that covers core competencies, assessment frequencies, and documentation requirements.</description>
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      <title>CAPA Workflow Best Practices for Compounding Pharmacies</title>
      <link>https://complirx.io/blog/capa-workflow-best-practices</link>
      <pubDate>Wed, 25 Mar 2026 00:00:00 GMT</pubDate>
      <guid>https://complirx.io/blog/capa-workflow-best-practices</guid>
      <description>Learn how to implement an effective CAPA workflow in your compounding pharmacy, from root cause analysis through effectiveness checks and documentation.</description>
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      <title>Preparing for Your First FDA Inspection: A Step-by-Step Guide</title>
      <link>https://complirx.io/blog/preparing-first-fda-inspection</link>
      <pubDate>Sat, 28 Mar 2026 00:00:00 GMT</pubDate>
      <guid>https://complirx.io/blog/preparing-first-fda-inspection</guid>
      <description>A comprehensive guide to preparing for your first FDA inspection, covering the 6-system inspection approach, pre-inspection preparation, common 483 observations, and building an always-ready culture.</description>
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