The Application of Disinfectants and Sterilants to Control Microorganisms; FDA Endotoxin Test Understanding the Latest Revision 2015 is a seminar that covers topics such as:
- Determining the vendor qualification requirements
- Determining the implementation aspects of a cleaning and disinfection program
- Determination of how application schedules apply to commissioning of a facility and after a shutdown
- How to develop an application schedule
- Impact of product expiration dating and regulatory implications
- The impact of sanitizers, disinfectants and sporicides on various common microorganisms found within a pharmaceutical facility
- The regulatory expectations of sanitizers, disinfectants and sporicides
- The use of coupons and liquid suspensions their advantages and disadvantages
- Resistance and rotation of disinfectants and its meaning to facilities
- Monitoring and interpretation of the results of the cleaning and disinfection program
The Application of Disinfectants and Sterilants to Control Microorganisms; FDA Endotoxin Test Understanding the Latest Revision 2015 brings together:
- Product Development
- Manufacturing
- Quality Assurance
- Project Management
- Regulatory Affairs
- Quality Control
- Validation
- Regulatory Compliance
