Environmental Monitoring in Pharmaceutical Production

Environmental monitoring In pharmaceutical production from SGS – important routine monitoring for clean room validation.

Ensuring that your clean rooms are uncontaminated is vital. We perform acceptance tests for the installation of clean rooms in production facilities as well as important routine monitoring of viable and non-viable contamination of your production facilities.

Our Life Science Services offers you a broad range of environmental monitoring services for clean rooms and can also provide you with customized hygiene-monitoring programs that suit your needs.

Services include:

• Viable and non-viable particle counting of air samples in manufacturing, packaging and testing sites
• Microbial sampling and enumeration of surfaces
• Cleaning validation studies
• Disinfectant efficacy studies
• Microbiological tests on individual process media (air, water and technical gases)
• Determination
• Determination of bacterial count in the air under all operating conditions
• Particle measurement
• Determination of total organic carbon (TOC)
• Media control, such as humidity, particle, oil and organic residues in gases
• Testing surfaces, consumables and primary packaging
• Qualification of production facilities after installation, reconstruction and standstill, etc.
• Confirmation of personal hygiene, determination of microbiological exposure on clothing and hands or production personnel

Contact SGS today to learn how we can help with your environmental monitoring requirements.