Requirements and environmental monitoring in pharmaceutical production versus operating rooms in hospitals with focus on airborne particles and microorganisms
Journal article, 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

Author

Catinka Ullmann

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

European Journal of Parenteral and Pharmaceutical Sciences

26336588 (ISSN) 17406277 (eISSN)

Vol. 20 3 100-103

Areas of Advance

Building Futures (2010-2018)

Subject Categories

Civil Engineering

More information

Latest update

8/8/2023 6