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

Författare

Catinka Ullman

Chalmers, Bygg- och miljöteknik, Installationsteknik

Bengt Ljungqvist

Chalmers, Bygg- och miljöteknik, Installationsteknik

Berit Reinmüller

Chalmers, Bygg- och miljöteknik, Installationsteknik

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

Styrkeområden

Building Futures

Ämneskategorier

Samhällsbyggnadsteknik

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2017-10-07