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Water Purification Systems for Regulated Industries
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Water Purification Systems for Regulated Industries

The course consists of interactive lectures, discussions, and imbedded exercises. Participants will also be placed in several real life situations where they complete a compliance review of a schematic process flow diagram, analyze failures using trend reports, critique a risk assessment, and perform a change control analysis including the impact of requested or proposed modifications.

6/25/2015 to 6/26/2015
When: June 25-26, 2015
9:00 a.m. - 3:00 p.m.
Where: The Desmond Hotel and Conference Center
1 Liberty Blvd
Malvern, Pennsylvania  19355
United States
Presenter: The Center for Professional Innovation & Education, Inc.
Contact: Olivia Carlin
610.648.7550

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Water Purification Systems for Regulated Industries - Design, Chemistry and Validation

The course consists of interactive lectures, discussions, and imbedded exercises. Participants will also be placed in several real life situations where they complete a compliance review of a schematic process flow diagram, analyze failures using trend reports, critique a risk assessment, and perform a change control analysis including the impact of requested or proposed modifications.

The course is designed to provide the attendee with a practical understanding of the following topics:

  • Basic water chemistry
  • Water quality selection criteria
  • EPA, EU, and WHO drinking water standards
  • The governing regulatory agencies with direct impact on water systems
  • Analytical water grades (1, 2, 3) and reagent water types (I, II, III, IV, with A, B & C subgroups)
  • Pharmacopeia water grades (Purified, Highly Purified, Water for Injection & Clean Steam)
  • Pretreatment component equipment – selection and operating principals
  • Final treatment options (reverse osmosis, vapor compression, single-effect and multiple-effect stills)
  • Opportunities for energy and water resource conservation
  • Point of use criteria such as temperature, location, time-of-day, and demand (GPM & GPD)
  • System design including materials of construction, generation, storage and distribution options
  • Trend reports (analysis, problem identification, predictive value)
  • Control systems, data historian, secure access, set points and alarms
  • Managing performance deviations and component failure
  • Direct and in-direct impact analysis
  • Quality by design including risk assessment
  • Instrument calibration for critical, non-critical, and informational only devices
  • Maintenance impacts to system performance, reliability, and validation
  • The importance of as-built documentation – user and field directed changes 

Learn more about the course and register.

CfPIE is a preferred provider and offers MichBio members a 15% discount on course registration fees. Click here for more information.

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