Biocontainment in pharmaceutical manufacturing plays a critical role in keeping patients, personnel, and the general public safe from potentially harmful contaminants. This course will give you a foundational comprehension of the different levels of biocontainment, outline actionable best practices, and leave you with an understanding of key regulatory concerns.
Environmental Monitoring (EM) is a critical component to ensuring microbial contamination control in pharmaceutical product development, research, and manufacturing settings. Using a risk-based approach to EM can save money while improving efficiencies and product quality. This webinar will show you how.
This course provides practical information on contamination control and clean room management. Information is presented for the critical daily aseptic maintenance and housekeeping functions necessary to maintain required cGMP cleanliness levels.
This course reviews how quality systems help define requirements for aseptic techniques and cleanrooms and how to properly maintain these environments.
Whether you need a foundation for cleanroom microbiology or are looking for a refresher, this course will outline critical components and current best practices.
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