Marya's air conditioning unit passes FAT for pharmaceutical cleanroom in Equador

Published: 20-Jun-2024

Marya’s cleanroom air conditioning unit has passed factory acceptance testing for a major client in Ecuador

Marya, a China-based sterile solution provider, has provided its client with an air conditioning unit that has passed factory acceptance testing.

Its client is Ecuador-based and is one of the largest pharmaceutical companies in South America, it mainly produces analgesics, anti-inflammatory drugs, antibiotics, respiratory and digestive system drugs, and various vitamins.

The specifications were: 

Industry: pharmaceutical

Cleanroom class: D

Cleanroom area: 2500 square cleanroom +8000 square warehouse

Product description: Air-cooled heat pump and direct expansion machine of HVAC engineering, jet fan cabinet, electrical engineering, etc.

Applicable industries: pharmaceutical factory, warehouse, etc.

GMP requirements are important to ensure that the cleanroom environment meets the requirements of pharmaceutical manufacturing and other processes, and complies with relevant regulations and standards.

The client's requirements were different air conditioning units for different plant areas and uses.

Marya delivered solutions including:

  • Direct expansion machine
  • Air-cooled heat pump
  • Jet fan cabinet

All of which can save energy and meet the client's different needs.

This cleanroom turnkey project required varying humidity levels

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 was an important milestone for Marya in this project as it demonstrated the performance of its cleanroom air conditioning units met the client’s requirements and standards.

This cleanroom turnkey project required varying humidity levels:

  • Humidity to be 18 to 25 celsius 
  • Humidity less than or equal to 48%
  • Humidity less than or equal to 65%

The number of air changes was required to be 20 to 25 times per hour which was fully in line with GMP requirements. 

GMP requirements are important to ensure that the cleanroom environment meets the requirements of pharmaceutical manufacturing and other processes, and complies with relevant regulations and standards.

The cleanroom air conditioning unit for the pharmaceutical factory in Ecuador was successfully shipped at the end of May 2024.

Its client is Ecuador-based and is one of the largest pharmaceutical companies in South America

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 familiarise themselves with and operate the system.

Marya’s construction team will ensure the installation quality and performance of the system and will provide the necessary training and support to the client.

 

Image credit: Marya

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