Veolia Water Technologies & Solutions

Take the downtime out of your cleaning validation program.

Go from days to minutes for equipment release time with Process Analytical Technology (PAT)

Sievers M9 TOC Analyzers can easily integrate directly online with your CIP skid to provide real-time, validated data with the highest degree of data integrity, process understanding, and process control. Avec des gains d’efficacité et des rapports transparents, vous obtenez une évaluation complète de la propreté avec moins de risques d’erreur.

Cleaning Validation is an integral component to GMP manufacturing to ensure safety and purity of products. With PAT and automation, you have the opportunity to build quality and efficiencies into your program and decrease human interaction, OOS investigations, and equipment downtime.

  • Eliminate room for human error
  • Redeploy analyst resources
  • Use validated, real-time data to make decisions, optimize your process, and troubleshoot
  • Assess the real-time rinse down profile of your process
  • Leverage 3 key quality metrics for process understanding - inorganic carbon, TOC, and conductivity

Our team of CV experts are ready to help:

  • Assess your current program for compliance and opportunities for PAT
  • Assess the feasibility and scope of transitioning to online cleaning validation
  • Conduct real-time soiling and cleaning studies

Interested in online cleaning validation? Let us know and we'll come to you.

Whether it's volume, pressure, location, or time constraints, we can assess feasibility and solutions for your CV program.

 

App Note: Online Cleaning Validation for Real-Time Equipment Release

online cleaning validation for real-time equipment release

This application note outlines Veolia's solution for online cleaning validation using the Sievers M9 Analyzer for TOC and conductivity integrated with a Clean-in-Place (CIP) skid. La validation du nettoyage en ligne permet une meilleure compréhension et un meilleur contrôle du procédé, une meilleure gestion des risques, des gains d'efficacité et une optimisation qui ne peuvent pas être obtenus par un contrôle en laboratoire. This aligns with the FDA's Process Analytical Technology (PAT) approach for operational efficiencies and lean processes.

Read App Note