Pharmaceutical production versus operating rooms in hospitals with focus on airborne particles and microorganism - Requirements and environmental monitoring
Paper in proceedings, 2016

Clean areas used for aseptic manufacturing of sterile medicinal products are subject to governmental requirements and guidelines in order to minimize 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.ultraclean air operating rooms including environmental monitoring with focus on particle and microorganism levels.

Author

Catinka Ullman

Chalmers, Civil and Environmental Engineering, Building Services Engineering

Bengt Ljungqvist

Chalmers, Civil and Environmental Engineering, Building Services Engineering

Berit Reinmüller

Chalmers, Civil and Environmental Engineering, Building Services Engineering

International Symposium on Contamination Control, ICCCS, Sao Paulo, Brazil, sept 2016

Areas of Advance

Building Futures (2010-2018)

Subject Categories

Civil Engineering

More information

Created

10/7/2017