What is the difference between ISO 14644 and GMP classifications?
Many companies have an ISO cleanroom. Far fewer have a GMP-compliant manufacturing environment. The difference isn’t in the walls. It’s in the data integrity, validation and lifecycle control behind them. Read more [Picture source: ABN Cleanroom Technology NV on linkedin.com]
Meet DryCell
The plug & play dryroom from ABN Cleanroom Technology designed for R&D and pilot-scale environments requiring ultra-low humidity conditions. Read more [Picture source: ABN Cleanroom Technology NV on linkedin.com
Cleanroom data is the new battleground
Everyone is talking about AI. But AI without trusted data is just expensive fiction. In cleanrooms, we already generate massive amounts of data every single day: temperature, relative humidity, pressure cascades, airflow, energy consumption, alarms, door movements, HVAC performance, filter behavior. The real question is never do we have data? The real question is: can we…
AI will not fix poor cleanroom data
Data in cleanrooms is massively underestimated. Not because there is too little data. But because we too often assume that the data is correct, complete and reliable. And that is exactly where the problem starts. AI does not fix bad data. It amplifies it. Read more [Picture source: ABN Cleanroom Technology NV…
Construction milestone reached for CWS Cleanrooms project in Dublin
ABN Cleanroom Technology, in collaboration with Brecon Cleanroom Systems, has reached a construction milestone for two new ISO Class 5 and ISO Class 7 cleanroom suites for CWS Cleanrooms in Dublin. Read more [Soucre: cleanroomtechnology.com]
Does a dryroom require a different approach than a cleanroom?
The core difference: A #cleanroom controls airborne particle concentration, classified under ISO 14644-1. A #dryroom controls dew point, the temperature at which moisture condenses from the air. Standard cleanroom HVAC systems cannot reach the dew point levels required for battery or advanced materials manufacturing. Read more [Picture source: ABN Cleanroom Technology NV…
How often should a cleanroom be validated?
Validation frequency is not just a matter of time. It is a matter of control and should always be defined in detail in your validation master plan (VMP). A Validation Master Plan contains a high-level document that outlines the overall strategy, approach and resources for validating systems, equipment and processes. Read more…
Do you always need humidity control in a cleanroom?
Humidity control is not explicitly required by cleanroom standards such as ISO14644, which primarily focus on particle concentration. However, in practice, humidity control is often essential to ensure stable and reliable cleanroom operation. Humidity directly affects product quality, equipment performance and operator behaviour. Without proper control, variations can compromise the integrity of the controlled environment. Its…
ABN Cleanroom Technology and Brecon deliver two new cleanrooms for Aalberts Advanced Mechatronics
The cleanroom specialists have teamed up to provide Aalberts Advanced Mechatronics with two new cleanrooms. Read more [Source: cleanroomtechnology.com]
What makes a cleanroom expensive (for the wrong reason)?
Cleanrooms often become expensive not because of technology, but because every project starts from scratch every single time. In many traditional projects, engineers redesign airflow concepts, pressure cascades, control strategies and wall systems again and again. As a result, specifications tend to accumulate without always questioning what the process truly requires. Read…