Auditing for Microbiological Aspects in Pharmaceutical Manufacturing 2018 is a webinar that covers topics such as:
- 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
Auditing for Microbiological Aspects in Pharmaceutical Manufacturing 2018 is intended for:
- Manufacturing Departments
- Quality Departments
- Regulatory Departments
- Engineering Departments
- Contract Manufacturing Organizations
- Microbiologists
