ATSPL's extensive technical knowledge and experience in clean room design coupled with our steadfast commitment to quality and the highest standards of customer service provide our clients with reliable, accurate and thoroughly documented clean room results, ensuring optimal clean room performance, documented regulatory and quality compliance, and minimized facility down time.

The engineering team has excellent knowledge and experience for implementing critical HVAC systems for pharmaceutical production facilities. Our experience covers all project kinds, sizes and their phases (CD, BD, DD, DR, DQ, C, IQ and OQ). Our intimate knowledge of processes and their GMP requirements make us the ideal partner for working HVAC and cleanroom solutions.

The environmental conditions have a strong impact on product quality in any pharmaceutical facility.In order to achieve Good Manufacturing Practice (GMP) cleanrooms, we applies the Society for Pharmaceutical Engineering’s (ISPE) guidelines, ASHREA, ISO guidelines. We are thoroughly familiar with GMP regulations such as EU, USFDA and WHO cGMP.