01Cleanroom Construction
Design and build of classified cleanroom environments — walls, ceilings, flooring and airlocks engineered to ISO 14644 standards.
ISO Class 5–8Modular PanelsAirlocks & Pass-throughsEpoxy Flooring
02HVAC & Validation
Pharmaceutical-grade HVAC with full qualification — temperature, humidity and pressure cascade control, HEPA filtration and documented IQ/OQ/PQ.
HEPA FiltrationPressure CascadesIQ/OQ/PQEnvironmental Monitoring
03Purified Water Systems
Generation, storage and distribution systems for PW, HPW and WFI — sanitary design, orbital welding and full documentation.
PW / WFISanitary PipingStorage & DistributionSampling Points
04Process Piping & Utilities
Clean utilities and process piping — clean steam, compressed air, nitrogen and CIP/SIP systems installed to GMP requirements.
Clean SteamCompressed AirCIP/SIPOrbital Welding
05GMP Compliance & Qualification
Documentation and turnover packages aligned with GMP guidelines — from design qualification through performance qualification.
DQ/IQ/OQ/PQAs-built DocumentationSOP SupportRegulatory Readiness
06Electrical & Automation for Pharma
Clean-area electrical fit-outs, BMS/EMS integration and 21 CFR Part 11-ready monitoring for critical environments.
Clean-area FixturesBMS/EMSData LoggingAlarm Management
