PROCESS VALIDATION & CONTINUED PROCESS VERIFICATION - Europe

Making the life science industry a safer place…and loving every minute of it! We have spent the past three decades on an epic ride through the life science industry. With early beginnings in the FDA and globally-regulated environment, we understand the importance of exchanging knowledge to make drugs and devices safer, and equipment and processes more scientifically sound. In the end, exchanging knowledge not only improves lives, but also saves them. Whether you attend one of our interactive conferences or webinars, or take advantage of our valuable free process documents; our goal is to provide tools and techniques that will have an instant impact on your core responsibilities.

Knowledge Exchange Network

Process Validation & Continued Process Verification (CPV)


<h3>Process Validation &amp; Continued Process Verification (CPV)</h3> 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:<ul><li>Walk through a risk-based implementation case study</li><li>Master the Validation Master Plan (VMP)</li><li>Establish a compliant Continued Process Verification (CPV) process</li><li>Uncover the top 5 challenges</li><li>Leverage technology transfer and engineering studies</li><li>Discover a Quality by Design (QbD) approach</li><li>Process Performance Qualification (PPQ) - Select the optimal sampling plan</li><li>Develop a gap analysis checklist for your program</li><li>Understand how to use statistics in process validation</li><li>Learn an effective approach for combination products</li></ul> Personnel in the Following Environments Should Attend:<ul><li>Validation</li><li>QA/QC</li><li>Engineering</li><li>Regulatory Affairs</li><li>Compliance</li><li>Manufacturing</li><li>Laboratory</li></ul> This event is also appropriate to business development and sales managers that offer innovative solutions for change control, risk management, statistics and validation.

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PROCESS VALIDATION & CONTINUED PROCESS VERIFICATION - Europe

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