The course addresses environmental monitoring for the manufacturing of both sterile and non-sterile products. It looks at the legislation and guidance available, techniques employed to monitor pharmaceutical environments, data trending and how to manage out of limit results.
Additionally a review of risks associated with contamination sources, monitoring methods,
trending and reporting of results is undertaken. This course is aimed at personnel in production
and quality functions who wish to increase their understanding of regulatory requirements and
expectations for the environmental monitoring of pharmaceutical operations.
Additionally a review of risks associated with contamination sources, monitoring methods,
trending and reporting of results is undertaken. This course is aimed at personnel in production
and quality functions who wish to increase their understanding of regulatory requirements and
expectations for the environmental monitoring of pharmaceutical operations.
