Clean Room Monitoring

The microbiological, bio-technological and pharmaceutical sectors are subject to GMP requirements, with testing and validation of clean room ventilation as one the most critical parameters. It is important to choose a consultant that has unique knowledge and experience in this field. Spectro has well-experienced consultant for testing and validation of clean rooms. We prepare the necessary protocols, perform the tests and make the final reports. Our experience with meeting the stringent requirements within the microbiological, bio-technological and pharma sectors can with advantage be transferred to other industries, such as hospitals, electronics, the food sector and the device industry.

Clean Room Monitoring Cover

	H.E.P.A. filter leak monitoring
	Airflow Particle Count monitoring
	Airflow Differential Pressures monitoring
	Airflow Volumes and Air Change rates
	Suite/room fabric integrity
	Noise and Light lux monitoring
	Airflow visualization display monitoring
	Temperature and Humidity checks