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Continued Verification * Master Planning * Risk * Statistics * Change Control * Data Integrity

March 30, 2020 - April 1, 2020

Philadelphia, United States

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.




More Information To Follow Soon



  • Since 1949, Ellab is a leading manufacturer of a full line of wireless, real-time data loggers and wired thermocouple validation systems with temperature, humidity, pressure, vacuum, conductivity and CO2 sensor options. Additionally, Ellab offers temperature standards, calibration dry blocks and liquid baths, custom fittings, accessories, and thermocouples. We also offer on-site qualification, validation and calibration services for thermal validation processes ranging from -196°C to 400°C. Typical environments often include -80°C freezers, incubators, stability chambers, autoclaves, and ovens.
    Website: https://www.ellab.com/


    More Information To Follow Soon



March 30, 2020
April 1, 2020
Event Category:


Wyndham Philadelphia Historic District
400 Arch Street
Philadelphia, PA 19106 United States
+ Google Map
(215) 923-8660

Pricing & Registration

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