Application of Disinfectants and Sterilants to Control Microorganisms; FDA Endotoxin Test – Understanding the Latest Revision

The Application of Disinfectants and Sterilants to Control Microorganisms; FDA Endotoxin Test – Understanding the Latest Revision 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 brings together:

  • Product Development
  • Manufacturing
  • Quality Assurance
  • Project Management
  • Regulatory Affairs
  • Quality Control
  • Validation
  • Regulatory Compliance

Future Events

Application of Disinfectants and Sterilants to Control Microorganisms; FDA Endotoxin Test – Understanding the Latest Revision 2020

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

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