Before cleanroom validation, a cleanroom requires mechanical calibration. HVAC calibration first ensures that the room meets the performance parameters which would deliver the expected results during final ISO validation, such as differential pressure, air change rates, and uniform airflow distribution.
In this post, we overview technical considerations for clean room fan filter unit selection, installation, and features. You’ll learn how PAC approaches design and configuration
In medical device cleanrooms, a common configuration is an ISO 8 gowning room and ISO 7 primary production area. A cascading air flow design and
How is a medical device cleanroom built? Here’s a component-by-component guide to ISO Class 7 cleanroom construction.
There are a few options available to cleanroom facilities who require new upgrades for USP 800 compliance. The best option will depend on the variables
What equipment and engineering controls do USP 800 cleanrooms require? What types of storage and monitoring systems will I need?
For communication satellites that remain within earth’s orbit, an ISO Class 6-8 cleanroom allows sufficient particle and contaminant control. Cleanroom engineers design each space so that particles from production surfaces are whisked away from critical components. A combination of softwall production areas and hardwall cleanroom facilities provide isolation of critical tasks.
Pre-engineered fabrication consolidates scheduling with minimal disruption and fewer variables. Difficult or expensive upgrades avoid overbearing noise, construction artifacts, and minimize if not eliminate the burden on facility staff for project management.
New USP guidelines may present challenges for compounding facilities. Some facilities need infrastructural and mechanical modifications for compliance. System evaluation includes duct systems, HEPA fan filters, differential pressure standards, air monitoring, and external air exhaust equipment.
Definitive Cleanroom Construction FAQ: How much does a cleanroom cost? How does the level of ISO classification impact build and operating costs? How much supporting space will I need for a cleanroom addition or ISO class upgrade? What’s the advantage of a turnkey cleanroom system?
CleanPro’s turn-key cleanroom solution provided a one-stop, one-contact result for the initial delivery and on-site installation of walls, ceiling grids, electrical systems, flooring, filters, HVAC, and more.
This cleanroom and adjacent gowning area helped this customer prevent outer contamination from entering classified spaces.
Here are some best-in-class cleanroom projects, in which the PAC cleanroom division, CleanPro, provided expertise and turnkey execution for design and installation of cleanroom enclosures, furniture, and components.
What are the key determinants of cleanroom components? Learn about different types of cleanroom filtration, wall construction, lights, temperature, humidity and more.
Advantages for Modular Hardwall Design and Construction of ISO 14644-4 Cleanrooms.
There are numerous considerations when evaluating cleanroom construction and design. The goal of this post is to touch on the basics. You may very well
This article covers each key for adjusting load calculations, planning exfiltration paths, and angling for adequate mechanical room space relative to a cleanroom’s ISO class and certification.
