Over 20 years of experience in Sterile, Biological Pharmaceutical and Hospital Facilities Engineering Design, Construction and Validation.
Low temperature cleanroom design challenges and key points to consider: avoid condensation, stratification and energy-related issues....
In this post, we are going to see how to implement calculations for cooling and dehumidification in Excel....
Commissioning is defined as a quality-oriented process for verifying and documenting that the performance of facilities, systems and assemblies meets defined objectives and criteria....
Cleanroom air balance calculation. Air flows considerations to completely define cleanroom HVAC....
In this post, we are going to talk about particularities of the Heat gains in the Pharmaceutical HVAC that differs slightly from other HVAC applications....
Air Handling Unit Factory Acceptance Test is a part of the HVAC validation life cycle. It consists of documented testing of the AHU at the vendor facility. The goal is to check that meets all the specifications before at the manufacturer site....
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....
