Over 20 years of experience in Sterile, Biological Pharmaceutical and Hospital Facilities Engineering Design, Construction and Validation.
In this post, we'll explore the key considerations involved in designing HVAC fumigation systems for pharmaceutical facilities....
In this post, we are going to see how to implement calculations for cooling and dehumidification in Excel....
User Requirement Specifications (URS) is a mandatory GMP document, according to EU GMP Annex 15, 21 CFR Part 11, PIC/S, and other agencies....
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....
