Completing every step, CAI Engineering combines a full range of services starting from Consulting, Design and Construction (EPC), Comissioning, Qualification&Validation (CQV) and after-sales service. which customers can choose the service according to their needs
Completing every step, CAI Engineering combines a full range of services starting from Consulting, Design and Construction (EPC), Comissioning, Qualification&Validation (CQV) and after-sales service. which customers can choose the service according to their needs
Before starting the project Understanding the needs of customers and designing them to meet their requirements in accordance with the standards is the most important thing. CAI Engineering takes into account 4 important factors as follows:
At this stage, the customer will receive Conceptual Design and Price Estimation. We will divide the service model into 3 types, details as shown in the picture below.
Panel Expert : Wall Panel,Celling Panel ,Door Panel ,Glazing and Coving
Finishing Expert : Vinyl Flooring, Epoxy self Levering, Furniture Installation, Silicone Sealing
HVAC Expert : From full scale, bespoke Air Handling Units to Upflow units and Air distribution including air filtration system
Electrical Expert : Lighting, Power distribution, Communication system, Fire safety and interlocks system
Piping service: Compressed Air, Steam, Gases and Vacuum piping
Water Expert: Purified, WFI, Pure steam and Process Hot Water and Drainage
Monitoring Expert: Fully Networked Environmental Monitoring System (EMS) with IT integration with 21CFR part11 compliance, BMS and IOT
Electrical Expert : Lighting, Power distribution, Communication system, Fire safety and interlocks system
Piping service: Compressed Air, Steam, Gases and Vacuum piping
Water Expert: Purified, WFI, Pure steam and Process Hot Water and Drainage
Monitoring Expert: Fully Networked Environmental Monitoring System (EMS) with IT integration with 21CFR part11 compliance, BMS and IOT
( Commissioning , Qualification and Validation)
The key point after the construction is completed is to operate the system according to the design and pass the cleanroom standards such as ISO14644, PIC/S for the pharmaceutical industry, etc.
Commissioning : It is the most important part before the delivery of the work. Because the implementation of the system according to the design must be done by a team with specialized experience in HVAC and cleanroom.
Qualification : For pharmaceutical cleanrooms (Pharmaceutical Cleanroom) will have the steps of the document. Qualification& Validation Master Plan(QMP & VMP)more added A risk assessment document based on the PIC/S requirements will be produced, including Installation Qualification(IQ), Opetational Qualification(OQ). ) and Performance Qualification(PQ ) from experience in building more than 20 cleanrooms
( Commissioning , Qualification and Validation)
The key point after the construction is completed is to operate the system according to the design and pass the cleanroom standards such as ISO14644, PIC/S for the pharmaceutical industry, etc.
Commissioning : It is the most important part before the delivery of the work. Because the implementation of the system according to the design must be done by a team with specialized experience in HVAC and cleanroom.
Qualification : For pharmaceutical cleanrooms (Pharmaceutical Cleanroom) will have the steps of the document. Qualification& Validation Master Plan(QMP & VMP)more added A risk assessment document based on the PIC/S requirements will be produced, including Installation Qualification(IQ), Opetational Qualification(OQ). ) and Performance Qualification(PQ ) from experience in building more than 20 cleanrooms
( Commissioning , Qualification and Validation)
The key point after the construction is completed is to operate the system according to the design and pass the cleanroom standards such as ISO14644, PIC/S for the pharmaceutical industry, etc.
Commissioning : It is the most important part before the delivery of the work. Because the implementation of the system according to the design must be done by a team with specialized experience in HVAC and cleanroom.
Qualification : For pharmaceutical cleanrooms (Pharmaceutical Cleanroom) will have the steps of the document. Qualification& Validation Master Plan(QMP & VMP)more added A risk assessment document based on the PIC/S requirements will be produced, including Installation Qualification(IQ), Opetational Qualification(OQ). ) and Performance Qualification(PQ ) from experience in building more than 20 cleanrooms
By clicking “Accept”, you agree to the storing of cookies on your device to enhance site navigation, analyze site usage, and assist in our marketing efforts. Privacy Policy
