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What is the qualification dossier (DQ, IQ, OQ, PQ)?

Explore the qualification dossier (DQ, IQ, OQ, PQ): What is it? Discover the process and benefits of ensuring cleanroom equipment quality in accordance with GMP standards.

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EN 1822 standard for HEPA H13, H14, and ULPA U15 filters

The EN 1822 standard for HEPA H13, H14, and ULPA U15 filters helps optimize cleanroom systems by ensuring efficient air filtration and production safety.

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Requirements for Cleanroom Equipment Meeting EU GMP Standards

Specialized requirements for EU GMP compliant cleanroom equipment, including design, materials, cleaning, disinfection, validation, and risk management, ensure optimal product quality in the...

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Guide to Designing a Cleanroom that Meets ISO Class 5 Standards.

Anh Khang Cleanroom provides comprehensive cleanroom solutions that meet ISO Class 5 standards through a rigorous technical process.

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EU-GMP Standards and the Differences from WHO-GMP Standards

The differences between these two standards and the cleanroom requirements in pharmaceutical manufacturing. Let's explore the benefits of complying with these quality standards for medical products.

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ISO 14644-6:2007 (National Standard TCVN 8664-6:2011)

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ISO 14644-5:2004 - Cleanroom Standard

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Everything You Need to Know About ISO 22000

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ISO 14644-4:2001 - Cleanroom Design and Construction Standard