On-demand webinar: Microbiological control in a pharmaceutical manufacturing environment
This webinar will address the evaluation of microbiological, environmental monitoring data as well as what would be considered significant differences in data.
We will review microbiological trending and how it can assist in understanding what is significant in each particular situation. We discuss how the analysis of this trended data enables a company to establish alert and action levels as well as methods for determining these levels. We will review cleaning validation protocols, methods, and procedures to evaluate and define a robust program to protect your products, personnel, and equipment. Finally, water is perhaps the most extensively used raw material in pharmaceutical manufacturing. Its use as an inactive ingredient, active pharmaceutical ingredient (API), analytical reagent, and even as a solvent in cleaning processes, leads to potential product and environmental contamination from residual water impurities.
Analytical techniques, Biologics, Biopharmaceuticals, Bioprocessing, Data integrity, Endotoxin, Environmental Monitoring, Good Manufacturing Practice (GMP), Manufacturing, Microbiology, Outsourcing, QA/QC, Regulation & Legislation, Research & Development (R&D), Supply Chain