Laboratory Water Systems: Necessary Water Specifications and Validation Challenges

GlobalCompliancePanel, a leading regulatory and compliance continuing education training provider, will organize a RAPS pre-approved webinar on the topic, “Laboratory Water Systems: Necessary Water Specifications and Validation Challenges” on October 23.

Online PR News – 05-September-2012 – Online Training – Description:Not many pharmaceutical businesses appreciate the criticality of water systems to their testing. Lab water can make or mar a lab test, because the quality of water determines the outcome in unseen ways. Depending on the quality of water; good tests pass off as bad ones, and vice versa.
Despite its importance, lab water gets relegated to the peripheral aspects of a pharmaceutical business. This is because many pharmaceutical businesses do not understand its role in quality tests. This webinar will give participants a clear understanding of the importance of water in their testing and facilities.
Pharmaceutical businesses sometimes end up doing either of these: Not getting a thorough understanding of water systems when they need to, the reasons for which are discussed in this webinar, and putting too much effort into their water systems when it is not required. They need to strike the right balance, because getting their priorities right on water systems goes a long way in helping them be in good business health. This webinar will enable them to achieve this balance. It will offer them way by which to make a science-based decision on what water quality is needed for the analyses as well as to remain compliant with regulatory expectations.
This webinar covers the following areas:
 What quality do you really need?
 Required attributes
 Perhaps unnecessary attributes
 Lab water supply options
 Lab water system design issues
 Lab water system validation
 Needed or not?
 Customized to attributes of importance
 Packaged water options and issues

When:October 23, 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. (, and since becoming a full time consultant, has served consumer products and FDA-regulated industries with training and troubleshooting expertise. The areas he has covered include water systems, sterilization, aseptic processing, microbiological and beta-lactam contamination control and microbiological laboratory operations. Soli has also served as a pharmaceutical expert witness in several "contamination" litigations.

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
o Validation managers and personnel
o Engineers involved in water system design and installation
o Personnel and their managers involved in maintaining laboratory water systems
o QA managers and Regulatory Affairs personnel involved in defending lab water system operations and quality data to FDA and EMA inspectors and outside auditors
o QC laboratory managers and personnel involved in sampling, testing, and trending data from lab water systems
o QC analysts and their supervisors who use the lab water
o Consultants and Trouble-shooters
Duration: 90 minutes
To enroll for this webinar, contact
Phone: 800-447-9407

Contact Information
Wilmington Delaware, 19801