Virtual Training 2021 - Aseptic Process Validation : Critical for compliance and success Virtual Training

Cleanroom classifications and the techniques for proper cleaning and disinfection are presented; along with a high-level overview of microbiology in regards to cleanroom environmental monitoring and the associated impact to product and patient health and safety.
Explain the difference between Aseptic and Bulk processing
Understand facility and personnel requirements necessary to maintain microbial control
• The role of environmental monitoring
• Types & sources of microorganisms
• The impact of microorganisms on product and patient health and safety
Speaker:
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations.