Curtailing Microbial Excursions and Investigations in Pharmaceutical Water Systems

Overview:

Water system microbial excursions are the bane of laboratories, utility operations, and production, often causing huge expenditures of labor for system sanitization and additional testing and quarantines of whole systems or specific outlets while fruitless investigations are mounted, not to mention the potential cost of product rejections when root causes are not definitive.

Though some excursions are real and a sign of system control problems, most are probably self-inflicted, being caused by poorly designated "trigger values", poorly designed use points, or poorly executed sampling or testing. This presentation will explore these possible causes, including the symptoms of real (as well as false) water system problems, and provide effective alternatives to avoiding most of your current superfluous excursions, as well as how to build supporting data useful in pinpointing causes when investigations are indeed necessary.

Why Should You Attend: When was the last time you performed a water system excursion investigation and could not definitively conclude the root cause? If you are like most firms, this scenario was probably your most recent experience, happens quite often, and frankly, is probably completely unnecessary. Most excursions are usually caused by self-inflicted phenomena. This presentation will discuss the most common causes of microbial excursions in water systems and how they can easily be avoided with minimal effort. Just think of the resources, production downtime, product losses, and cost you could save by making a few rational changes to your action "trigger values", sampling and testing, while still being able to (more clearly now) see real system problems when they do occur. You simply cannot afford to not tune in to this valuable webinar!

Areas Covered in the Session:

• What are excursions? 
• Water system dilemma: process control or quality control (utility or raw material), or both 
• Intended functions of Alert/Action Levels and Specifications 
• Investigation, necessary and often fruitless 
• Excursion responses and impact 
• Criticality of valves, hoses, & outlet flushing 
• Diagnosing the source of the problem 
• Minimizing unnecessary excursion responses through best practices

Who Will Benefit: This webinar will be valuable for all companies that operate WFI or Purified Water systems, particularly for those in FDA and EMEA regulated industries, including Medical Devices, Diagnostics, Pharmaceuticals, and Biologics fields, as well as consumer products and cosmetics companies. The employees who will benefit include:

• QA managers and personnel involved in investigations of excursions and preparing CAPAs
• QC managers and personnel involved in sampling, testing, and trending chem and micro data from water systems
• Utility operators and their managers involved in maintaining and sanitizing water systems
• Validation managers and personnel
• QA managers and other personnel involved in Change Control programs
• QA managers and Regulatory Affairs personnel involved in defending water system operations and quality data to FDA and EMEA inspectors and outside auditors
• Consultants and Troubleshooters

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