€1,748.14 – €2,330.85

CLEANING VALIDATION & CRITICAL CLEANING PROCESSES - NOV 2019

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Cork

Ireland

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Design a Cleaning Program that Impresses Regulatory Investigators

A compliant cleaning validation program is essential for a successful regulatory inspection. Even today, many have struggled to develop effective processes and keep up with evolving sterile regulations that meet an inspector’s expectations. This conference is designed for those professionals in charge of developing, implementing and maintaining new or legacy cleaning validation programs. Attend this conference and walk away with the innovative processes, techniques and tools that have an immediate impact for your company and professional development.

Top 10 Reasons to Attend:

  1. Overcome the Top Five Cleaning Validation Challenges
  2. Understand EU Annex 1 Revisions – Your Guide to Sterile Manufacturing
  3. Implement a Risk-Based Cleaning Validation – Key Elements to a Successful Program
  4. Establish Acceptance Criteria and Health-Based Limits in Cleaning Validation
  5. Create Best-in-Class Cleaning Validation Documents – Master Plans, SOPs, Assessments, Technical Reports and More
  6. Develop Cleanroom Validation, Disinfection and Environmental Monitoring Procedures
  7. Manage Changes in Cleaning Validation Processes
  8. Use Advanced Analytical Methods for Cleaning Validation
  9. Set Critical Cleaning Process Parameters and Critical Quality Attributes
  10. Qualify Water Systems, Clean Steam Systems and Process Gasses

Personnel in the Following Environments Should Attend:

  • Validation
  • QA/QC
  • Engineering
  • Regulatory Affairs
  • Compliance
  • Manufacturing
  • Laboratory

This event is also appropriate for business development and sales managers that offer innovative solutions for quality, validation and engineering professionals in the life science environment.

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Cork

Ireland

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