Auditing for Microbiological Aspects in Pharmaceutical Manufacturing 2018

Topics

• What international regulations should be referenced
• Provide background information on what microbiological aspects to audit
• Validation and qualification of bioburden and manufacturing suites
• ISO classification of rooms and how it should be applied
• What the source means in terms of root cause
• Key sources of microorganisms and why this is important
• Product bioburden and why bioburden is important

Who should Attend

• Manufacturing Departments
• Quality Departments
• Regulatory Departments
• Engineering Departments
• Contract Manufacturing Organizations
• Microbiologists