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. Technical representatives from Cherwell will explain microbial air sampling options and implementation aspects and there will be a tour of Cherwell's manufacturing facility.

About our partner Cherwell Laboratories:

Cherwell Laboratories provides standard and bespoke cleanroom microbiology solutions that help customers effectively manage their controlled environments and processes. Established for over 45 years, the company has built a strong reputation as a leading supplier of Redipor prepared microbiological media and environmental monitoring equipment, with considerable expertise within the pharmaceutical and related industries.

• Understand the testing techniques regularly used in pharmaceutical production operations
• Know how to interpret results and identify trends
• Know what factors to consider when developing an environmental monitoring programme appropriate for your operations