Run in partnership with Environmental Monitoring Process Validation Specialists, Cherwell Laboratories, 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.
The course agenda includes Technical Representatives from Cherwell explaining Microbial Air Sampling options, implementation aspects and the classroom course also includes a tour of Cherwell's manufacturing facility.
The course agenda includes Technical Representatives from Cherwell explaining Microbial Air Sampling options, implementation aspects and the classroom course also includes a tour of Cherwell's manufacturing facility.
