Knowledge Base
Welcome to the Angstrom Technology Knowledge Base — your dedicated resource for delving deep into the intricate world of cleanroom solutions. Here, we’ve curated an abundance of articles, guides, and resources to empower you with comprehensive insights into the technicalities of contamination control.
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ISO 14644 Cleanroom Requalification
Ongoing Performance Qualification requires a repeat of the initial testing on the cleanroom to…
Validation Frequency Requirements
How often do I need to validate a cleanroom? ISO 14644-2:2015 – Monitoring to…
HEPA and ULPA Air Filtration
HEPA and ULPA filters are tested during manufacture to EN1822:2019 and ISO 29463 test…
Vertical Farming
Crops are grown on many levels to maximise on available space, allowing the crop…
CBD Cleanrooms
There are two areas in which cleanrooms can support the production of cannabis-derived products.…
Particle Counter Calibration Service
Particle counter and monitoring equipment calibration service Book the calibration of Airy, Aerotrak, EMS,…
Glass Reinforced Polyester (GRP) Cleanroom Wall and Ceiling Systems
Glass Reinforced Polyester (GRP) creates an advanced cleanroom panel. No framework for doors or…
Cleanroom Commissioning
Factory Acceptance Test A Factory Acceptance Test (FAT) is a process that evaluates any…
Cleanroom Design Phase
Conceptual design Conceptual design is the very first stage of the cleanroom design process,…
Controlling contamination through an effective monitoring programme – Whitepaper
“Contamination within a cleanroom is caused by the non-intentional or accidental introduction of viable or non-viable…
Cell & Gene Therapy Suites
Cell and Gene Therapy The Cell and Gene Therapy catapult, which has the core…
GMP Requalification
Cleanroom Requalification is usually completed on an annual basis, however the revision of Annex…