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AI has moved from slide decks to the shop floor. Cameras now inspect vials. Models flag deviations before anyone opens a batch record. And regulators have noticed.  EU GMP Annex 22 is the first set of EU GMP rules written specifically for artificial intelligence in medicine manufacturing. If your quality team uses AI, or plans

As AI reshapes the life sciences industry, data security in the AI-driven environment has become the defining leadership challenge of our time. Every pharma executive, compliance officer, and quality leader is asking the same question: Can we trust AI with our most sensitive data? The answer is not a simple yes or no. It requires

GMP auditing serves as the cornerstone of pharmaceutical quality assurance and product safety. As we approach 2025, we’re seeing a growing emphasis on comprehensive audit processes that provide a big-picture look at organizational compliance with Good Manufacturing Practice regulations. These audits typically take  for simple assessments and up to ten days for complex manufacturing sites.