Engineered cleanroom environments tailored to the regulatory demands of each sector.
Typical Standard: ISO 4 to ISO 8 / GMP Grade A, B, C & D
Aseptic compounding suites, sterile fill-finish operations, and bioprocessing cleanrooms engineered to EU-GMP Annex 1 & FDA 21 CFR Part 211.
Typical Standard: ISO 1 to ISO 5 / N/A (Industrial Micro-tech)
Ultra-clean environments with sub-micron particle filtration, electrostatic discharge (ESD) mitigation, and Airborne Molecular Contamination (AMC) control.
Typical Standard: ISO 6 to ISO 8 / GMP Grade C & D compliant
Controlled environments for the precision assembly, packaging, and bioburden inspection of implantable devices and sterile disposables.
Typical Standard: ISO 5 to ISO 8 / N/A (High-precision technical)
Large-span cleanrooms with overhead crane integration, outgassing-free materials, and laminar airflow for satellite and laser optics assembly.
Typical Standard: ISO 5 to ISO 7 / GMP Grade B & C
Specialized containment suites, hospital sterile compounding pharmacies, and BSL-2/BSL-3 biocontainment laboratories.