Over 20 years of experience in Sterile, Biological Pharmaceutical and Hospital Facilities Engineering Design, Construction and Validation.
It is not necessary to explain here the importance of overpressure in pharmaceutical facilities. Is a GMP requirement to establish a differential pressure (normally 10-15 Pa) between cleanrooms and adjacent less clean spaces to avoid product contamination....
Outdoor condition selection is one of the preliminary design conditions we should determine. In many cases, this will be fixed by the customer, or by the regulations. In the Pharmaceutical Industry, outdoor design temperature and relative humidity can have an impact over the product quality...
