How to test the quality of CSM gloves is a key factor to ensure chemical safety and compliance in the pharmaceutical, chemical and cleanroom industries. With strong chemical resistance, high mechanical strength and outstanding ozone - UV resistance, CSM gloves need to be evaluated by CQ, CO, durability and chemical resistance.
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Comparing CSM and NBR gloves is an important step when choosing protective equipment for GMP-compliant pharmaceutical manufacturing environments. Each material has its own advantages and disadvantages in terms of durability, chemical resistance, cleanliness and suitability for each sterile area.
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CSM gloves are the premium choice in sterile areas of the pharmaceutical industry due to their strong chemical resistance, superior durability and suitability for isolators. As EU-GMP and WHO-GMP standards become increasingly stringent, CSM gloves become the optimal solution to protect compounding, filling and manufacturing processes for injectable
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From 2024–2026, the trend of clean factory design will change dramatically thanks to AI, IoT and smart sensor systems. These technologies help factories operate automatically, monitor the environment in real time and meet GMP – ISO 14644 standards in the context of transitioning to a smart factory model.
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In a cleanroom environment, cleanroom equipment maintenance is crucial to maintaining cleanliness, stability, and ISO 14644-GMP compliance. Regular inspections help ensure proper equipment operation, prevent breakdowns, avoid cross-contamination, and reduce the risk of audit failures.
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In the pharmaceutical industry, getting a cleanroom GMP design right from the start determines operational efficiency and the likelihood of achieving certification. Errors such as incorrect flow arrangements, inappropriate material selection, or lack of differential pressure control can delay a project or cause it to fail an audit.
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The cost of investing in a GMP cleanroom includes many more items than a normal construction project — from design, panel construction, HVAC system to GMP inspection, training and assessment. Understanding each item helps businesses accurately budget and avoid unexpected expenses when putting the cleanroom into operation.
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TCVN 7395-1 standard is an important technical foundation for the design and inspection of medical cleanrooms in Vietnam. Based on ISO 14644-1, this standard specifies the classification of air cleanliness, helping hospitals, laboratories and medical equipment factories maintain sterile environments that meet international standards.
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Pass Box cleaning is an important step to maintain cleanliness and prevent cross-contamination in cleanrooms. However, many units still make mistakes when cleaning improperly or using inappropriate materials, leading to reduced air filtration efficiency and potential cross-contamination risks in production.
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The cost of regular maintenance of pharmaceutical cleanroom air filtration systems is not only an investment to maintain stable operation but also a mandatory requirement according to GMP standards. Proper periodic maintenance helps prevent cross-contamination, prolongs equipment life and ensures safe drug quality.
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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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