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2015-10_annex15_0.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 Annex 15 (2015) provides detailed guidance on qualification and validation for pharmaceutical manufacturing, covering equipment, facilities, utilities, processes, and cleaning to ensure consistent product quality and regulatory compliance.

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