The cleanroom air conditioning unit of Ecuador pharmaceutical factory was successfully shipped at the end of May 2024.
The client’s team went to the factory in mid-May for pre-shipment factory acceptance testing (FAT) to test AHU performance and it passed successfully. This is an important milestone in demonstrating that the performance of cleanroom air conditioning units meets client’s requirements and standards.
This Reinraumprojekt requires room humidity to be 18 to 25 ℃, some rooms humidity is less than and equal to 48%, and the rest of the room is less than and equal to 65%. The number of air changes is required to be 20 to 25 times per hour which is fully in line with GMP requirements. Those are important to ensure that the cleanroom environment meets the requirements of pharmaceutical manufacturing and other processes, and complies with relevant regulations and standards.
In addition, the Marya construction team plans to go to Ecuador in July 2024 for system installation, commissioning and delivery, and will provide engineer training. This will ensure that the cleanroom air conditioning system will function properly after installation and that the client’s engineers will be able to familiarize themselves with and operate the system.
These plans and measures show that you have taken appropriate steps to ensure the successful delivery and operation of your cleanroom air conditioning system. The professional services of the Marya’s construction team will ensure the installation quality and performance of the system and we provide the necessary training and support to the client.
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