Over 20 years of experience in Sterile, Biological Pharmaceutical and Hospital Facilities Engineering Design, Construction and Validation.
User Requirement Specifications (URS) is a mandatory GMP document, according to EU GMP Annex 15, 21 CFR Part 11, PIC/S, and other agencies....
Analysis about where to locate fans in an air handling unit: blow thru (fan before coils) and draw thru (fan after coils)...
A typical example of desiccant calculation in Excel for pharmaceutical HVAC applications....
A few tips on energy savings in Pharmaceutical HVAC design and how to reduce energy consumption...
Low temperature cleanroom design challenges and key points to consider: avoid condensation, stratification and energy-related issues....
