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Ensuring compliance with stringent cleanroom regulations is crucial for maintaining product quality, safety, and efficacy in industries such as pharmaceuticals and biotechnology facilities. Vaporized Hydrogen Peroxide (VPHP) disinfection is a widely used method for decontaminating cleanrooms due to its efficacy in eliminating a broad spectrum of microorganisms. However, it’s critical to understand that physical cleaning is necessary for effective contamination control and regulatory compliance.
Join us for an insightful webinar on "The Regulatory Perspective on Cleaning and Disinfecting Isolators, Pass Boxes, and Other Minienvironments" where David Talmage, Vice President with PDA, will guide you through the essential regulatory requirements and best practices for cleaning and disinfecting cleanroom environments – from isolators to whole rooms – regardless of the method of microbial control and disinfection. Emphasis will be on PDA TR70, Eudralex GMP Annex 1, and USP<1072>.
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Vice President or Parenteral Drug Association (PDA)
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