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Follow on Google News | “Water System Bio-film Control and Microbial Monitoring Myths” from GlobalCompliancePanelAn unfortunate, yet undeniable fact of water systems is that many of them are designed keeping obsolete concepts in mind. The result of an organization’s reluctance to update its water systems is that the systems are built on a shaky foundation.
An unfortunate, yet undeniable fact of water systems is that many of them are designed keeping obsolete concepts in mind. The result of an organization’ This webinar will discussion some detail the reasons for which such fallacies happen, but greater attention will be paid to how these systems can be corrected. For this to happen, a few established myths have to be shattered. This session seeks to quell popular myths surrounding water systems, for most important reason for which water systems go awry. Most of these myths relate to microbial control approaches and microbial monitoring. The speaker brings his over three decades of experience in water systems in taking up each myth for demystification. This session will cover the following areas: o Why water myths develop: Impact of c-GMPs Well-meaning but misguided precedents Scientifically unchallenged traditions and benchmarking Rule-hungry culture o Water System Microbial Control Myths: WFI from RO Turbulent Flow and Flow Rate Dead Leg Rules Smooth Surfaces In-Line Sterilizing Filters Ozone o Microbial Enumeration Myths: Referee Methods Thermophiles in Hot Systems R2A, 35°C, 5 days Test Filter Membrane Rating Compendial Action Levels TOC and Endotoxin as Microbial Count Correlates ------------------------------------------------------------ When:February 5, 10:00 AM PDT | 01:00 PM EDT ------------------------------------------------------------ By whom: T.C. Soli is a Ph.D. Microbiologist and President of Soli Pharma Solutions, Inc. (www.solipharmasol.com) Prior to full time consulting, he had 25 years of diverse "Big Pharma" operating company experience. During his 31+ year career, he has lectured extensively at conferences, authored numerous papers and has recently written several book chapters related to water system microbiology for USP, PDA and ISPE publications. He is currently serving in his third five-year term on USP Expert Committees responsible for Pharmaceutical Waters through which he authored the complete rewrite of USP Chapter 1231, which many consider to be USP's "pharmaceutical water bible". ------------------------------------------------------------ For whom: The webinar will benefit 1. Validation managers and personnel 2. Engineers involved in water system design and installation 3. Utility operators and their managers involved in maintaining and sanitizing water systems 4. QA managers and Regulatory Affairs personnel involved in defending water system operations and quality data to FDA and EMEA inspectors and outside auditors 5. QA managers and personnel involved in investigations of excursions and preparing CAPAs 6. QC laboratory managers and personnel involved in sampling, testing, and trending chemical and micro data from water systems 7. Consultants and troubleshooters ------------------------------------------------------------ Duration: 90 minutes ------------------------------------------------------------ To enroll for this webinar, contact webinars@globalcompliancepanel.com Phone: 800-447-9407 End
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