Knowledge

10.07.2026

What Is the Difference Between a Dispensing Booth and a Sampling Booth?

Dispensing Booths and Sampling Booths are both used to control dust, reduce cross-contamination and create a suitable working environment for handling raw materials in pharmaceutical, dietary supplement, cosmetics, food and chemical manufacturing facilities. Because their physical construction and airflow principles may appear similar, the two types of equipment are often considered interchangeable.

10.07.2026

IQ, OQ and PQ Qualification Costs: Scope, Cost Factors and Reference Pricing

The cost of IQ, OQ and PQ qualification is an important part of the investment budget for cleanroom equipment, HVAC systems, production lines and controlled manufacturing facilities. The total cost is not determined solely by the purchase price of the equipment. It also depends on the qualification scope, applicable standards, number of tests, documentation requirements, measuring instruments, personnel and the possibility of repeat testing.

27.11.2025

How to check the quality of CAM gloves: CO, CQ, durability, chemical resistance

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.

27.11.2025

CSM vs NBR Gloves Comparison: Which is Suitable for Pharmaceutical Manufacturing?

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.

21.11.2025

Clean Factory Design Trends 2026: AI, IoT, Sensors

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.

21.11.2025

Checklist for maintenance of all cleanroom equipment

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.

21.11.2025

20 frequently asked questions when designing GMP cleanrooms

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.

21.11.2025

What is the minimum cost of investing in a GMP clean room?

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.

13.11.2025

Standard TCVN 7395-1:2004 – Foundation of clean rooms used in medicine

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.

12.11.2025

Common mistakes when cleaning Pass Box

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.

What Is the Difference Between a Dispensing Booth and a Sampling Booth?

IQ, OQ and PQ Qualification Costs: Scope, Cost Factors and Reference Pricing

How to check the quality of CAM gloves: CO, CQ, durability, chemical resistance

CSM vs NBR Gloves Comparison: Which is Suitable for Pharmaceutical Manufacturing?

Clean Factory Design Trends 2026: AI, IoT, Sensors

Checklist for maintenance of all cleanroom equipment

20 frequently asked questions when designing GMP cleanrooms

What is the minimum cost of investing in a GMP clean room?

Standard TCVN 7395-1:2004 – Foundation of clean rooms used in medicine

Common mistakes when cleaning Pass Box

Top read

What Is the Difference Between a Dispensing Booth and a Sampling Booth?

HVAC System Design for Multi-Product Manufacturing Facilities

IQ, OQ and PQ Qualification Costs: Scope, Cost Factors and Reference Pricing

Differences Between Pharmaceutical Cleanrooms and Electronics Cleanrooms

Vietnam Cleanroom

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