Air handling architecture, pressure cascades and documentation engineered for regulated manufacturing — from Grade A filling lines to Grade D support areas.
We separate fresh air treatment, process conditioning and return handling so each loop can be validated, serviced and balanced independently.
Handles 100% fresh air: pre-filtration, dehumidification, cooling and reheat, delivering stable conditions to the cleanroom loop regardless of outdoor climate.
Conditions recirculated air for the critical zone: terminal HEPA filtration, tight temperature and humidity control, and validated airflow for Grade A–C areas.
Manages return and extract streams, keeping the pressure cascade stable at 10–15 Pa between adjacent grades, with heat recovery where process air allows.
Every line of the regulation has a physical answer in the unit. This is the mapping we hand to your validation team.
Hygienic design, cleanability and documented contamination control strategy for Grade A–D manufacturing.
Airflow and filtration sized for the target classification, with filter integrity test ports fitted.
Pressure differential between adjacent grades maintained by volume tracking and damper control.
Particle, pressure, temperature and humidity sensors wired to the BMS with alarm history.
Documentation package: material certificates, weld records, test protocols and calibration data.
Stainless interior, flush welds, sloped drain pans, no dirt traps — VDI 6022 compliant.
Where AERO-M Pro handles comfort and industrial duties, MEDIC-AIR is the platform we build for audited environments — same modular logic, but every surface, joint and drain is designed to be cleaned and documented.
Unidirectional airflow modules over filling and aseptic processing lines,HEPA protected and monitored.
Dedicated extract handling for weighing, coating and solvent processes, with ATEX-conscious construction.
Background air handling with cascading pressure control and recovery time calculated for the room volume.
The same hygienic platform serves hospital projects: theatres with laminar ceilings, isolation rooms with defined pressure direction, and sterile corridors — all to DIN 1946-4 hygiene requirements.
N+1 fan arrays, dual power feeds on control circuits and free-cooling integration — sized for continuous duty and monitored round the clock.
High fresh-air rates, long duct runs and low specific fan power: comfort systems designed around the energy calculation, not around a catalogue page.
Yes. We size the supply and extract volumes with the room leakage in mind and control them with volume-tracking dampers. The control philosophy, sensor locations and alarm thresholds are part of the documentation pack.
We supply the documentation that supports your qualification: material certificates, weld maps, filter certificates, factory test records and O&M manuals. IQ/OQ protocols are prepared with your validation team.
Standard is AISI 304; AISI 316L is available for aggressive cleaning regimes or corrosive processes. Exterior is galvanised or coated steel unless otherwise specified.
Extract streams are handled separately with dedicated units, sealed casing and, where required, bag-in bag-out filter housings. We confirm the arrangement against your containment strategy.
Send the room schedule, grades and pressure cascade. We return a compliant equipment list and drawings while there is still time to influence the layout.