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…
GMPConnect Monitoring Software
In regulated industries such as pharmaceuticals, biotechnology, and medical devices, computerized systems are critical. Our cleanroom monitoring system help protect product quality, patient safety, and data integrity. At ABN Cleanroom Technology, we implement and validate GMPConnect using a proven risk-based approach. This ensures compliance…
Start your cleanroom project online
Tell us about your cleanroom requirements and specifications, and we’ll prepare a first cost estimation for you within one working day. Simply complete the form with as much detail as possible, from classification and size to specific industry or technical needs. Read more
Effective cleanroom facility management
Cleanroom facility Management is essential for industries requiring stringent contamination control, such as biotechnology, pharmaceuticals, and semiconductor manufacturing. Therefore, we cover everything from maintenance and process utilities to cleanroom furniture fit-out services. As a result, a well-managed and properly equipped cleanroom not only optimizes operational efficiency but also ensures regulatory compliance and enhances product quality.
We’re proud to contribute to the construction of one of Europe’s most sustainable cleanroom laundries for CWS Cleanrooms in Puurs, Belgium
At the heart of their new flagship facility lies our VIX® concept, where configuration intelligence drives ultra-low energy consumption. By dynamically adapting ventilation based on real-time process conditions, VIX® significantly reduces the environmental footprint of high-intensity cleanroom operations and supports CWS Cleanrooms in achieving their ambitious sustainability targets. This ISO 5 & ISO 7 certified facility…
The final phase of the +500m² cleanroom project
We’re entering the final phase of the +500m² cleanroom project for GC Europe in Leuven. After installing the orange filter lighting to protect sensitive materials during the production process, validation activities are now in full progress. Read more and watch…
CYTONIX™ – Modular cytostatics. Fully isolated. Ready to rent.
With the 2026 PIC/S regulations for Belgian hospitals coming closer, ABN Cleanroom Technology NV launches a turnkey rental solution for the production of cytostatics: CYTONIX™. Read more [Picture source: ABN Cleanroom Technology NV on linkedin.com]