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<title>GxP Frame Publications</title>
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<updated>2026-05-27T00:00:00Z</updated>
<author><name>Brian Drapeau</name></author>
<entry>
<title>The CDMO Training Crisis: Why the $52 Billion Cell &amp; Gene Therapy Market Can&#x27;t Scale Without Better Training</title>
<id>https://www.gxpframe.com/insights-cdmo-training-crisis</id>
<link href="https://www.gxpframe.com/insights-cdmo-training-crisis"/>
<published>2026-05-27T00:00:00Z</published>
<updated>2026-05-27T00:00:00Z</updated>
<summary>CDMO training is the bottleneck for cell and gene therapy growth. Why multi-client chaos and turnover break programs, and the architecture that fixes them.</summary>
</entry>
<entry>
<title>FDA CMC Flexibility for CGT Manufacturers: Here&#x27;s Why Most Will Use It Wrong</title>
<id>https://www.gxpframe.com/insights-fda-cgt-flexibility</id>
<link href="https://www.gxpframe.com/insights-fda-cgt-flexibility"/>
<published>2026-04-03T00:00:00Z</published>
<updated>2026-04-03T00:00:00Z</updated>
<summary>FDA CMC flexibility for cell and gene therapy is real, but it demands more process understanding, not less. Why most will misuse it and how to stay ready.</summary>
</entry>
<entry>
<title>Pharma LMS Implementation: Your LMS Is Either Your Greatest Asset or Your Most Expensive Filing Cabinet</title>
<id>https://www.gxpframe.com/insights-lms-greatest-asset</id>
<link href="https://www.gxpframe.com/insights-lms-greatest-asset"/>
<published>2026-02-13T00:00:00Z</published>
<updated>2026-02-13T00:00:00Z</updated>
<summary>Pharma LMS implementation and administration decide whether your LMS is a training asset or an expensive filing cabinet. Here is what good looks like.</summary>
</entry>
<entry>
<title>The SOP Authoring Trap: Why Your Procedures Don&#x27;t Work on the Floor</title>
<id>https://www.gxpframe.com/insights-sop-authoring-trap</id>
<link href="https://www.gxpframe.com/insights-sop-authoring-trap"/>
<published>2026-02-12T00:00:00Z</published>
<updated>2026-02-12T00:00:00Z</updated>
<summary>SOP authoring fails when the wrong people write for the wrong audience in the wrong format. Why procedures break on the floor and a better way to write them.</summary>
</entry>
<entry>
<title>AI Training in Biopharma: What&#x27;s Real, What&#x27;s Hype, and What You Need to Know Now</title>
<id>https://www.gxpframe.com/insights-ai-training-revolution-biopharma</id>
<link href="https://www.gxpframe.com/insights-ai-training-revolution-biopharma"/>
<published>2026-02-11T00:00:00Z</published>
<updated>2026-02-11T00:00:00Z</updated>
<summary>AI training in biopharma: a practitioner&#x27;s look at what is deployed, what is promising, and what is still hype, plus what training managers should do now.</summary>
</entry>
<entry>
<title>Why Your GMP Training Program Is a Ticking Time Bomb (And What to Do About It)</title>
<id>https://www.gxpframe.com/insights-training-time-bomb</id>
<link href="https://www.gxpframe.com/insights-training-time-bomb"/>
<published>2026-02-09T00:00:00Z</published>
<updated>2026-02-09T00:00:00Z</updated>
<summary>Is your GMP training program a ticking time bomb? What FDA Form 483s and warning letters reveal about training deficiencies, plus solutions that actually work.</summary>
</entry>
<entry>
<title>Building a Biotech Startup Training Program: A Survival Guide</title>
<id>https://www.gxpframe.com/insights-biotech-startup-training</id>
<link href="https://www.gxpframe.com/insights-biotech-startup-training"/>
<published>2026-02-07T00:00:00Z</published>
<updated>2026-02-07T00:00:00Z</updated>
<summary>Building a biotech startup training program without cutting corners: what to build first, what can wait, and the costly mistakes startups make later on.</summary>
</entry>
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