- Modernizing the Aseptic Process – An overview of aseptic processing, lifecycle approach and risk assessment and general guidelines for process simulations.
- Microbiology Testing for Non-sterile products – Risk-based assessments to determine acceptance criteria and determining objectionable organisms in non-sterile pharmaceutical products.
- Particulate Matter Testing – Testing requirements and methods for intravenous and parenteral products.
- Product Sterility Testing – Basic testing requirements and methods, isolator package validation requirements and Bacteriostasis and Fungistasis (B/F) requirements
- Container Closure Integrity Testing – Testing requirements, available methods and regulatory trends.
Nelson Laboratories To Conduct Pharmaceutical Microbiology Seminar
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