Requirements and environmental monitoring in pharmaceutical production versus operating rooms in hospitals with focus on airborne particles and microorganisms
Artikel i vetenskaplig tidskrift, 2015

Clean areas used for aseptic manufacturing of sterile medicinal products are subject to governmental requirements and guidelines in order to minimise risks of particulate and microbiological contamination. High cleanliness is also a necessity in hospital environments to ensure safe conditions for the patients. The requirements for premises within the pharmaceutical industry are compared to those of the hospital, e.g. operating rooms including environmental monitoring with a focus on particle and microorganism levels.

aseptic sterile production area

Envirionmental monitoring

ultraclean air operating room


Catinka Ullmann

Chalmers, Bygg- och miljöteknik, Installationsteknik

Bengt Ljungqvist

Chalmers, Bygg- och miljöteknik, Installationsteknik

Berit Reinmüller

Chalmers, Bygg- och miljöteknik, Installationsteknik

European Journal of Parenteral and Pharmaceutical Sciences

26336588 (ISSN) 17406277 (eISSN)

Vol. 20 3 100-103


Building Futures (2010-2018)



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