Cleaning Validation Summit 2017

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Are you compliant with FDA requirements for cleaning validation? Today’s regulators are applying more fine-grained specifications and demanding more sophisticated procedures for planning, executing, and documenting your processes throughout a drug product’s lifecycle. This two-day intensive summit brings together industry leaders to help you exceed regulatory thresholds and avoid costly FDA inspection findings.

Featuring Representation From:

• Amgen
• Bristol-Myers Squibb
• Novartis
• Steris
• MedImmune
• Bayer
• Akorn
• CPCI
• EcoLab
• Toxikon
• GSK
• And Many More!

Featuring Comprehensive Coverage On:

• Ensuring your Cleaning Program is FDA Audit Ready
• Cleaning Validation and Continued Process Verification
• Risk-Based Approaches to Cleaning Systems Design, Qualification and Ongoing Monitoring
• Cleaning Limits and Visual Inspection from the Analytical Perspectives
• Determine Cleanability and its Applications in Cleaning Validation
• Process Validation & Cleaning Strategies during Technology Transfer of Sterile Injectables
• EU GMP Changes and Its Impact on Cleaning Validation
• Quality by Design for Effective Cleaning Procedure
• Writing Cleaning Validation SOPs
• And much more!