Process Validation & Continued Process Verification (CPV)

Process Validation is the backbone of all validation and is always under FDA regulatory scrutiny. KENX is excited to announce the definitive process validation and continued process verification conference of 2019. This event gives you the tools and technology needed to create, deploy and maintain best practices through all three stages of validation. Come to Philadelphia this spring and align with best-in-class case studies that impress FDA investigators and make an immediate impact for your organization and professional career.

Top 10 Reasons to Attend:

• Walk through a risk-based implementation case study
• Master the Validation Master Plan (VMP)
• Establish a compliant Continued Process Verification (CPV) process
• Uncover the top 5 challenges
• Leverage technology transfer and engineering studies
• Discover a Quality by Design (QbD) approach
• Process Performance Qualification (PPQ) - Select the optimal sampling plan
• Develop a gap analysis checklist for your program
• Understand how to use statistics in process validation
• Learn an effective approach for combination products

Personnel in the Following Environments Should Attend:

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

This event is also appropriate to business development and sales managers that offer innovative solutions for change control, risk management, statistics and validation.