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EU GMP Volume 4 Annex 1 (2022).pdf

Jason Peng, an engineer at Deiiang Company

  • Author:Jason Peng

  • Cleanroom Engineering Technology Manager of Deiiang Company.

    Product R&D Manager of GDC Inc. Cleanroom Equipment Manufacturing Company.

    Executive Director of Guangdong Cleanroom Industry Association of China.

    Engaged in R&D of related products for 15 years, with rich relevant technical experience
  • 2026-07-26  |  Visits:

EU GMP Volume 4 Annex 1 (2022) sets out detailed regulatory requirements and guidance for the manufacture of sterile medicinal products, focusing on contamination control, cleanroom classification, and robust aseptic processing.

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