GMP & CSV compliant building automation
Market leader in Thailand's life-science sector for Building Automation Systems — supplying products, services and validation that satisfy GMP and CSV requirements.
- GMP compliant
- CSV documentation
- Clean room & HVAC
Validation-ready automation for regulated environments
We supply complete building automation for pharmaceutical, biotechnology and life-science facilities — from HVAC and clean-room pressure control to environmental monitoring — with the validation deliverables auditors expect.
- IQ / OQ / PQ documentation packages
- 21 CFR Part 11 friendly audit trails
- Clean-room differential pressure and temperature control
- Energy management that lowers operating cost
Compliance & Validation
Everything needed to pass an audit and stay compliant.
GMP Compliance
Systems designed and documented to Good Manufacturing Practice requirements.
CSV (Computer System Validation)
Validation master plan, risk assessment, protocols and traceability matrix.
HVAC & Clean Room Control
Temperature, humidity, pressure cascade and air-change control with alarms.
Energy Management Systems
Metering, dashboards and analytics to reduce energy consumption.
Environmental Monitoring
Continuous monitoring of critical parameters with secure historical records.
Life Safety & Access
Fire alarm integration, access control and emergency response sequences.
Validation lifecycle
URS Review
We translate your user requirement specification into a compliant design.
Design & Risk
Detailed design with risk assessment and traceability mapping.
IQ / OQ / PQ
Installation, operational and performance qualification executed and documented.
Change Control
Ongoing change control and periodic review to stay inspection-ready.
Building a regulated facility?
Let us prepare the automation and validation documentation your auditors expect.