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Remediating Pharmaceutical Water System Biofilm - What to Do After It Gets Ahead of You

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Date: 03-Jun-13 to 03-Jun-13
Location: Online Event / California City / California / United States
Category: Healthcare & Pharmaceuticals Conferences & Trade Fairs

This pharmaceutical water systems webinar training will discuss what you should do when your monitoring data tells you that you may have a significant biofilm problem. It covers how to verify that the data and your interpretation of the data are correct, as well as the location of the problem which gives you clues as to what caused the problem and its impact on manufacturing and product.

Visitors

This webinar will be valuable for all companies that operate WFI or Purified Water systems, particularly for those in FDA and EMA regulated industries, including Pharmaceuticals, Biotech and Biologics fields, as well as consumer products and cosmetics companies. The employees who will benefit include:
Validation managers and personnel
Engineers involved in water system design and installation
Utility operators and their managers involved in maintaining and sanitizing water systems
QA managers and Regulatory Affairs personnel involved in defending water system operations and quality data to FDA and EMEA inspectors and outside auditors
QA managers and personnel involved in investigations of excursions and preparing CAPAs
QC laboratory managers and personnel involved in sampling, testing, and trending chem and micro data from water systems
Consultants and Troubleshooters

Exhibitors

Dr. Teri C. ("T.C.") Soli ,Ph.D. is President of Soli Pharma Solutions, Inc, serving the Pharmaceutical, Biotech, Medical Device, Dialysis, Cosmetics and Personal Care Products and related equipment and instrument manufacturing industries with training, auditing, and troubleshooting expertise. He has over 32 years of combined pharmaceutical experience as a consultant as well as with operating companies such as DSM Pharmaceuticals, Glaxo Wellcome, Burroughs Wellcome, and Pfizer.

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