Environmental Monitoring in pharmaceutical manufacturing is a critical process that systematically tracks and analyses environmental conditions such as air quality, temperature, humidity, and particulate matter to ensure controlled environments remain within regulatory standards. This monitoring is vital for identifying potential sources of contamination, evaluating the effectiveness of control measures, and upholding product and process safety and quality. The collected data supports the implementation of corrective actions, preventative strategies, and ongoing improvements to maintain environmental integrity and comply with Good Manufacturing Practices (GMP), thereby minimising risk factors associated with pharmaceutical production.
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