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Laboratory Water Quality

 
  August 08, 2012  
     
 
ComplianceOnline, Online Event
2012-08-28


Why Should You Attend:

Maintaining appropriate quality of lab water systems is perhaps more important than many applications of manufacturing’s water systems. This is because the tests performed on manufacturing’s products can be affected by the lab water quality in insidious, hard to detect ways, which could cause perfectly good products to appear to fail testing or bad product to appear to pass.

This webinar will assist the attendees in logically investigating and defining the specific quality attributes their lab water systems need and not just default to manufacturing’s required water quality. The need or lack thereof to validate your water system will also be discussed along with how that validation may be very different from that employed for manufacturing’s water system. So you may not be doing enough for your water system or you might be going well overboard. Using packaged waters and/or small self-contained water purification systems are often considered alternatives to having and maintaining a full-fledged water system, but these water sources must also meet all compendial water quality requirements. They have unique and often unrealized challenges that may make them less cost effective than thought.

 Areas Covered in the Seminar:

  • 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
Event Details:
 
Date:                    August 28, 2012
Time:                    10:00 AM-11:30 AM PDT
Cost:                    $249 per attendee per computer terminal
Registration:         SIgn-Up on-line now.  Add to your shopping cart.

 

 
 
Organized by: ComplianceOnline
Invited Speakers: 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. Dr. Soli’s career-long experience with water systems and product and process contamination troubleshooting, coupled with USP, ISPE, PhRMA, and PDA committee involvements, afford him practical knowledge and troubleshooting skills with contamination control, cleaning, sterilization, sterile and non-sterile processes, validation, laboratory testing, excursion investigations and all aspects of high purity water systems.
 
Deadline for Abstracts: 2012-08-28
 
Registration: http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=702398?channel=hummolgen
E-mail: referral@complianceonline.com
 
   
 
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