Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing 2018 is an event dedicated to total Organic Carbon (TOC) as a useful analytical method for cleaning validation studies, including design.
Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing 2018 covers topics such as:
- Description of analytical approaches in different instruments
- Principles of Total Organic Carbon Analysis
- Setting limits based on TOC
- Reasons for using TOC and Situations where TOC is preferred
- Grouping strategies for Analytical method validation
- Use of blanks and controls
- Cautions to be taken in sampling and analysis
- Dealing with interferences and Optimization of TOC recovery for difficult to oxidize or solubilise compounds
- Regulatory issues
- Use of TOC throughout the validation lifecycle
Total Organic Carbon Analysis for Cleaning Validation in Pharmaceutical Manufacturing 2018 intended for:
- QC Analysis Technicians
- QA and QC managers
- Operations managers
- Disinfectant validation managers
- Clean room managers
- Manufacturing operators
- Personnel and contractors that clean and disinfect clean rooms
- Clean room operators
- EH&S managers
- Regulatory compliance managers and environmental monitoring managers
- Validation Engineers and Specialist
