The most universally applied method for cleanroom classification is the one suggested in 1963 by Federal Standard 209 of the USA.  In this standard the number of particles equal to and greater than 0.5 µm is measured in one cubic foot of air. This count is then used to classify the room (1 particle = class 1; 10 particles = class 10…). In the same period, scientific publications concerning healthcare facilities suggested that airborne particles carrying micro-organisms associated with human disease were usually found in the 4-20 µm equivalent diameter range. This contamination can be detected by settle plates.

Historically, cGMP guidelines highlighted their expectations concerning a microbiological continuous process monitoring in A and B grades (FDA guideline_2004 and Annex 1_2008) by referring to settle plates because no other technology was easily available. Unfortunately, settle plates are a non-validatable method as the method is simply based on the physical principle of the downfall of a particle on a surface.

This webinar will consider the use of active air versus passive air settle plate monitoring in routine environmental monitoring on the basis of actual scientific knowledge.