Over 20 years of experience in Sterile, Biological Pharmaceutical and Hospital Facilities Engineering Design, Construction and Validation.
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....
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....
