Engineered cleanroom environments tailored to the regulatory demands of each sector.
Typical Standard: ISO 4 to ISO 8 / GMP Grades A, B, C & D
Aseptic compounding suites, sterile fill-finish operations, and bioprocessing cleanrooms engineered to EU-GMP Annex 1 and FDA 21 CFR Part 211.
Typical Standard: ISO Class 1 to ISO Class 5
Sub-micron particle filtration, electrostatic discharge (ESD) mitigation, and Airborne Molecular Contamination (AMC) control for wafer manufacturing and microelectronics.
Typical Standard: ISO Class 6 to ISO Class 8 (ISO 13485)
Controlled environments for the assembly, packaging, and bioburden inspection of implantable medical devices, catheters, and sterile diagnostic kits.
Typical Standard: ISO Class 5 to ISO Class 8
Large-span cleanrooms with overhead crane integration, outgassing-free materials, and laminar airflow for satellite and laser optics assembly.