Cleanroom engineering

Clean room engineering refers to the design, construction, and operation of clean rooms—controlled environments that minimize the introduction, generation, and retention of airborne particles, as well as controlling other parameters like temperature, humidity, and pressure.

Cleanroom design

The design of a clean room must adhere to strict standards and guidelines to ensure optimal cleanliness and functionality.They are essential in various industries, including pharmaceuticals, biotechnology, electronics, and aerospace, where even minute levels of contamination can compromise product quality and safety.

Cleanroom Construction

Cleanroom construction involves creating an environment designed to maintain specific cleanliness standards, typically utilizing specialized materials, air filtration systems, and strict procedures.

Cleanroom Testing

Cleanroom testing is a critical process that ensures products manufactured or tested in a controlled environment meet specific cleanliness and quality standards.

Cleanroom Certification

Cleanroom certification is a systematic process used to validate that a cleanroom meets specific cleanliness and environmental control standards.

Cleanroom Airflow

Cleanroom airflow is a critical aspect of cleanroom design and operation, as it directly influences the cleanliness and overall performance of the environment. T

CGMP Cleanrooms

A CGMP cleanroom refers to a cleanroom that is designed, constructed, and maintained according to the guidelines set forth by Current Good Manufacturing Practices (CGMP).

Semiconductor cleanrooms

​Semiconductor cleanrooms are highly controlled environments used in the manufacturing of semiconductor devices, such as integrated circuits (ICs) and microchips.

Electronic Cleanrooms

Electronic cleanrooms are controlled environments specifically designed to maintain a high level of cleanliness to support the production and assembly of electronic components and devices, such as semiconductors, integrated circuits, printed circuit boards (PCBs), and other sensitive electronic parts.

Modular CleanRoom

Clean work shed is an air purification equipment that can provide a local high clean environment. It is mainly composed of frame, acrylic, mesh soft curtain, FFU fan, high efficiency filter, lamps, etc.

Air Shower

Deiiang Purifier" Air shower room (AIR SHOWER) is also called air shower, clean air shower room, purification air shower room, air shower room, blow shower room, air shower door, dust bath room, blow shower room, air shower channel, air blow shower room.

Downflow Booth

Negative Pressure Weighing Room \Weighing Hood\Weighing Room\Negative Pressure Sampling Room (Center Weighing Room, Weighing Room) is a type of air purification equipment that provides a localized class A environment with localized negative pressure;

Clean bench

The clean bench is a box-type air purification equipment that can provide a local dust-free clean, sterile working environment class 100 (ISO class 5) local operating environment.

Air Filter

One of the components of air conditioning, air conditioning filters are mainly used for air conditioning for machine rooms, pre-filtration of ventilation systems, purification air conditioning clean room return air filtration, pre-filtration of high-efficiency filtration, pre-filtration of air compressors.

Electronic Cleanrooms

Electronic cleanrooms are controlled environments specifically designed to maintain a high level of cleanliness to support the production and assembly of electronic components and devices, such as semiconductors, integrated circuits, printed circuit boards (PCBs), and other sensitive electronic parts.

The role of GMP

Good Manufacturing Practices (GMP) play a crucial role in ensuring the quality and safety of products in various industries, particularly pharmaceuticals, cosme...

Cosmetic GMP Standards and Regulations

Good Manufacturing Practices (GMP) are critical to the cosmetic industry, ensuring that products are safe, effective, and of high quality.

Comply with GMP guidelines

Good Manufacturing Practices (GMP) are essential to ensuring product quality and safety in various industries, particularly pharmaceuticals, food, and cosmetics...

GMP Certification

Good Manufacturing Practices (GMP) certification is crucial for organizations seeking to ensure the quality, safety, and efficacy of their products.

Specific standards of GMP

According to GMP guidelines, facilities must be designed to prevent contamination.

5 Key Components of Good Manufacturing Practices

Good Manufacturing Practices (GMP) are essential for ensuring the consistent quality and safety of products in various industries, particularly pharmaceuticals,...

Difference between GMP and cGMP

Good Manufacturing Practice (GMP) refers to the established guidelines and regulations that ensure products are consistently produced and controlled according t...

Process for compliance with GMP standards for food and drugs

Good Manufacturing Practice (GMP) standards ensure that products such as food and pharmaceuticals are consistently produced and controlled according to quality ...

What is ISO Class 8 Cleanroom

​ISO Class 8 Cleanroom is one of the cleanroom categories defined by the international standard ISO 14644-1. This standard provides clear specifications for cle...

ISO 14644-5Operations

According to market research, implementing standardized operational procedures in clean rooms can enhance efficiency by up to 30% and reduce contamination risks...

ISO 14644-4: Design, Construction and Start-Up

According to statistics, the global cleanroom market is expected to reach US$4.16 billion by 2025, with an average annual growth rate of about 6.5%. Therefore, ...

ISO 14644-3: Test Methods

This article will analyze the primary test methods outlined in ISO 14644-3, focusing on air velocity, air pressure, and particle count, while incorporating rele...