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    <description>Short, practical notes on radiopharmaceutical QC, GxP documentation and the industry news that affects them.</description>
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      <title>The Part 212 rewrite missed its target date again</title>
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      <pubDate>Sun, 25 Oct 2026 12:00:00 +0000</pubDate>
      <category>Regulation</category>
      <description>The Food and Drug Administration&#x27;s Part 212 rewrite was due as a proposed rule in 09/2026 and hasn&#x27;t appeared. What it would change, and what labs can check.</description>
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