Static electricity – an overlooked element in cleanroom design that can cause fires and explosions, destroy electronic components, attract dust causing cross-contamination and erroneous measurements. Although little noticed, static electricity is a potential hazard that directly affects the safety, accuracy and quality of products in cleanrooms.
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Common errors when using asynchronous FFU often come from the difference in wind speed, pressure and operating time between the devices. This makes the air flow in the clean room unstable, causing cross-contamination and wasting energy. This article will analyze the causes and effective solutions.
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In cleanrooms, airflow is a decisive factor in the level of cleanliness and efficiency of HVAC. So, comparing airflow standards: ISO 14644 vs ASHRAE, what is the difference? This article will analyze the role, scope of application and complementarity of these two standards in the design and operation of cleanroom systems.
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In pharmaceutical production, the choice of applying WHO-GMP or EU-GMP greatly affects business strategy and target market. So when should WHO-GMP be used instead of EU-GMP? This article will analyze the differences, advantages and disadvantages and suggest suitable choices for businesses.
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In cleanroom design, the choice of standard is a key factor to ensure effective airflow control. This article analyzes the differences between ISO 14644 and ASHRAE standards, helping businesses and engineers understand the differences in air cleanliness classification, ventilation design, air velocity and air supply efficiency.
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P1, P2, P3, and P4 laboratories are classified according to biosafety standards (BSL) to ensure safety when researching microorganisms and dangerous viruses. Discover the differences in design, equipment, protection levels, and practical applications of each biosafety level to build laboratories that meet WHO and CDC standards.
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In today’s modern manufacturing and construction industries, metal surface treatment plays a critical role. A proper coating not only protects metals from corrosion, oxidation, and mechanical wear but also enhances aesthetics and ensures long-lasting durability.
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In the pharmaceutical, food, electronics or cosmetic industries, building a clean room that meets standards is a mandatory requirement to ensure safety and legal compliance. However, not all standards are suitable for all fields. This article will analyze How to choose the right Clean Room Standard System for each industry.
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In pharmaceutical and cosmetic production, many businesses mistakenly believe that a cleanroom meeting ISO 14644 is enough to meet GMP. In fact, ISO 14644 only focuses on controlling airborne dust particles, while GMP covers the entire production system. So why is ISO 14644 not enough to meet GMP and what else do businesses need to prepare?
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7 quality management tools are tools used to aim to grasp your problems more proactively and effectively. So what are these 7 tools? Please find out through the article below of VCR.
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Vietnam Cleanroom
Vietnam Cleanroom is a leading company in providing cleanroom equipment for contractors in Vietnam
Ha Noi Office: No.9, lane 675 Lac Long Quan, Tay Ho Ward, Ha Noi, Viet Nam
Ho Chi Minh Office: 15/42 Phan Huy Ich, Tan Son Ward, Ho Chi Minh City, Viet Nam
Hotline:
Service Feedback: 094.903.0817
Email: [email protected]
North:
+ Lane 279 Phuc Loi, Phuc Loi Ward, Ha Noi
+ Thien Loc Village, Ha Noi
Central: 42 An Duong Vuong Street, Vinh City, Nghe An Province
South:
+ Road 48, group 40, Hiep Binh Ward, Ho Chi Minh City
+ 104/4 Cho Chieu Street, Ho Nai 3 Ward, Dong Nai Province
Factory: Vinh Phu Village, Phu Tho Province
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