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A Guide to Getting Ahead of Changing Cleanroom Disinfectant Regulations and Building a Forward-Thinking Program

Make the switch ebook cover

Major regulatory actions, e.g., the U.S. EPA PTAP Data Call In and revisions to EU GMP Annex 1 – Manufacture of Sterile Medicinal Products illuminate a clear trend: Regulators are requiring pharmaceutical manufacturers to make significant changes to the products and processes used in cleanroom disinfection. This short eBook gives you a detailed outlook on what global regulatory changes mean today — and what they signal for the future. Get clear insights on how to build a forward-thinking cleanroom disinfection program and achieve key goals:

  • Create a global, sustainable portfolio
  • Streamline future global compliance
  • Improve operational efficiency
  • Protect cleanroom equipment
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