Total Organic Carbon measurement is a required test for pharma water and is regulated by USP and other pharmacopeia. Information can be misleading when it comes to what is required, and what meets regulatory compliance.

The importance of what is fact and what is incorrect has an impact on what methods are used to monitor TOC- differentiating from what is needed for validation requirements and providing better process control, risk mitigation, and more accurate proactive monitoring in manufacturing.

This discussion will directly dispel myths and false claims about compliance in pharmaceutical waters with specific focus on TOC and conductivity.

In this webinar you’ll learn:

• Answers to common questions to distinguish actual pharmacopeial requirements for pharmaceutical waters vs what has become widely accepted in the industry for TOC and conductivity
• Status of harmonization of pharma waters, test changes for sterile waters and more
• The impact real-time release testing of pharma waters for TOC on risk mitigation and process control
• Details of a TOC system designed to meet regulatory requirements

Who should attend:
Water process engineers, QA, QC, metrologists and persons responsible for system operation and analytical instrument selection, operation/maintenance