The definition of a clean room is a room in which the number of airborne particles is kept to a minimum using artificial means. These rooms are used in the semiconductor and chip industry, pharmaceutical and food industry, and also in electronic device manufacturing. The small particles in the ambient air that pose no danger to humans can still damage, contaminate or even destroy products from the aforementioned industries. There are many different types of cleanrooms. The right type for you will depend on many factors, including size, application, and the type of room you need to convert.
At SHP, our top priority is to provide you with the cleanroom that fits your exact needs. Whether your process requires lS0 14644-1 or GMP standard from IS0 3 to l0 8(Class A to Class D), we have the tools, materials, and knowledge to design a cleanroom that will satisfy your needs. Our cleanrooms can be constructed in a variety of ways, and can incorporate existing building walls, or can be free-standing within your facility. We have more than 20 years of experience in the cleanroom industry, which means we know what you need, and we can get it to you quickly.
SHP follows a proven formula to ensure success, Every project , no matter how complex , is thoroughly analyzed, innovatively planned and then executed to the highest standard. After a series of lean production in our own quality-controlled factories, our team guides you with collaborative approach through every step of the construction process, We carefully review your requirements, provide value-engineering opportunities and seamlessly integrate products, which minimizes cost and production times, Our implementation and project management strategy includes coordination with all trades in the field to ensure certainty of quality and on-time completion.
Our team will work with you, assessing your needs to build a custom testing schedule. To determine the most appropriate cleanroom validation tests, we'll consider factors such as:
ISO standard or GMP guideline requirements
Validation frequency requirements, including annual and interim testing
Your URS, risk assessment and monitoring plan
Tests will also depend on which cleanroom lifecycle phase needs qualification, including:
Installation Qualification (lQ)-meeting user and design requirements
Operation Qualification (00)-operating within the defined conditions
Performance Qualification (PO)- producing the defined results
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