BMS with open architecture and Lonworks / Bacnet compatible DDCs Pharma Suite : 21 CFR Part 11 compliant validation software.
As an engineering solutions provider, GMP takes responsibility for design, supply, installation, commissioning and maintenance, offering end-to-end solutions, energy management and comfort throughout the life-cycle of the system.
Our BMS design conforms to 21 CFR Part 11 and GAMP 5 requirement. This ensures control of different parameters like Relative Humidity (RH), Temperature, Pressure zoning etc. of a cleanroom in critical areas like production facilities, laboratories and sterile areas etc.
Smart PC touch panels in the production area are used to display critical Parameters. These parameters are monitored and recorded to keep a track record of manufacturing areas.
A central monitoring and controlling system installed at a central location provides control and real-time monitoring of critical parameters. This system is password protected at various levels ensuring tamper proof with data. Our technology partners like ALC, GE Security & DISTECH Controls ensure that our clients get the promise of quality and easy service across the globe. BMS professionals at GMP are trained and experienced in handling massive and critical projects such as sterile facilities where environmental monitoring is of utmost importance.