Cleaning Validation is a crucial component of an effective GMP Compliance program at any regulated drug manufacturing facility. During the last years, it has been one of the most evolving and debated topics in the pharma industry.

This event offers you a unique possibility to explore the current status and efficient implementation techniques of Cleaning Validation Guidelines.

Through the practical presentations and case studies from industry experts, you will examine the best practices of cleaning validation challenges relating to quality aspects, cleanroom technologies, and environmental monitoring considerations.

Program Highlights:

• Emerging regulations and new compliance standards

• Cleaning process development,
• Contamination control strategy,
• Grouping products and equipment for cleaning validation,
• Risk-based cleaning validation monitoring,
• Future of cleanroom design

Who Should Attend:

• Cleaning Validation
• Cleanroom Technology
• Aseptic Processing
• Sterile Technology
• Microbiology
• Microbe Monitoring and Control
• Technical Services
• Contamination control
• Manufacturing Science & Technology
• Process Monitoring and Control
• Environmental Monitoring
• Toxicology
• QA/QC
• Risk Management
• Regulatory Affairs