2-Day In-Person Seminar Comprehensive Seminar on Everything You'd Like to Know about Pharmaceutical Water Systems, But were Afraid to Ask


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This course is a comprehensive training on pharmaceutical water systems encompassing over 15 different course subjects and modules. The modules include design, build, installation, validation, regulatory compliance, regulatory audit expectations, documentation expectations, modules on continuous electro deionization (CEDI), ozone, reverse osmosis (RO), distillation methods, pure steam generation, pretreatment options, microbial mitigation and sanitization methods, raw water and sourced water criteria, instrumentation for both observational and compendial criteria, and automation expectations.

Microbial mitigation is one of the most important aspects for purification systems. This course emphasizes the mitigation of microbial in Purified Water and WFI water systems. Profiling microbial in pretreatment systems is a non-compendial exercise. There is a contentious debate about microbial counts in the pretreatment system and whether investigations should be conducted to find microbial considered part of the “bad bug” list. Profiling microbial in the pretreatment and whether this operation is warranted or not due to the new ISO-22519. How ISO-22519 applies to compendial compliance or not.

Modules will be given on WFI water systems produced by non-distilled means using a variety of purification modules to achieve WFI quality. Depiction of different product options for non-distilled WFI is will offered and analyzed. Additionally, there will be an overview module on the Baseline Guide for Water and Steam Systems, the most comprehensive guide on pharmaceutical water and steam systems in existence.

Examples of modules to be given at the seminar:

  • Annex 1 and its Comparison to Compendial mandates: What does it all imply to the industry
  • Comparison of Hot water, Chemical, and Ozone Sanitization for Pharmaceutical Processes
  • Continuous/Electro Deionization (CEDI)
  • Instrumentation, Measurements, Testing of Source, Pretreatment, and Pharmaceutical Waters
  • Lessons Learned from and In-depth FDA Investigation
  • Microbial Issues and its Mitigation in Pharmaceutical Waters
  • Myths, Misconceptions, and Realities: The Legacy of Obsolete SOPs and Specifications in Modern Pharmaceutical Water Systems
  • OPEX and CAPEX The Actual Cost Pharmaceutical Water Systems
  • PAT (Process Analytical Technology): An FDA and Industry Effort
  • Possible ideas, approaches, and directions for future production, process, cGMP compliance, and critical utilities
  • Production of WFI Water Without Distillation - New Changes in the European Pharmacopeia
  • Rapid Microbial Monitoring: Regulatory and Application Strategies for Pharmaceutical Water Systems
  • Source Water Microbial and TOC Destruction in Pretreatment Pharmaceutical Water Systems
  • Sustainability - The Reclaim, Recycle, Reuse and Reduction of Water in Biopharmaceutical Production
  • The Use of Statistical Process Control (SPC) and Exponentially Weighted Process Statistics (EWPS) for PAT in Pharmaceutical Water Systems
  • Understanding and Troubleshooting Pharmaceutical Water Systems
  • Validation of a Pharmaceutical Water System for the 21st Century
  • Water for Injection (WFI): A Changing Paradigm of Production Methods – USP Perspective
  • Water for Pharmaceutical Use / Water Purification Engineering

Learning Objectives:

You will learn and understand the following:

  • Pharmaceutical Water systems
  • The operations of a pharmaceutical water system
  • The basic chemistry involved in water purification
  • The options of choosing properly defined equipment for individual purification steps
  • The issues of microbial monitoring and sampling
  • The value of different sanitization methods used in pharmaceutical water systems
  • The difference between gram-negative and gram-positive bacteria and their influence in biofilm development
  • The configuration of CEDI, EDI, and Ion Exchange is removing ions from the water
  • The usage of microfiltration (MF), ultrafiltration (UF), and nanofiltration (NF)
  • All modules used in pharmaceutical water production from source water to finished product water supplied to production.
  • The different regulatory, pharmacopeial, and international regulatory issues associated with pharmaceutical water.
  • What lessons can be learned from a regulatory audit or investigation?
  • The usage of Statistical Process Control and Exponentially Weighted Process Statistics to monitor and control your water system long before it hits an action or alert limit.
  • The usage and production of non-distilled WFI.

Who will benefit:

Pharmaceutical, Over-the-Counter, Beauty, Nutraceutical, Biotechnology, and medical device industry professionals in engineering, critical utilities, technical competencies, maintenance, quality control, quality assurance, engineering management, global responsible production personnel.

DAY 01(9:00 AM - 5:00 PM)
  • 9:00 AM- 9:15 AM Registration Meet & Greet.
  • 9:15 AM- 10:00 AM
    • Instrumentation, Measurements, Testing of Source, Pretreatment, and Pharmaceutical Waters
  • 10:00 AM- 10:30 AM
    • Lessons Learned from an In-depth FDA Investigation
  • 10:30 AM- 10:45 AM COFFEE BREAK
  • 10:45 AM- 11:45 AM
    • Microbial Issues and its Mitigation in Pharmaceutical Waters
  • 11:45 AM- 12:30 PM
    • PAT Vs. Traditional Validation
  • 12:30 PM- 1:30 PM Lunch
  • 1:30 PM- 2:30 PM
    • Understanding and Troubleshooting Pharmaceutical Water Systems
  • 2:30 PM- 3:00 PM
    • Possible ideas, approaches, and directions for future production, process, cGMP compliance, and critical utilities
  • 3:00 PM- 3:15 PM COFFEEE BREAK
  • 3:15 PM- 4:00 PM
    • Rouge Monitoring
  • 4:00 PM- 4:45 PM
    • Rapid Microbial Monitoring: Regulatory and Application Strategies for Pharmaceutical Water Systems
  • 4:45 PM- 5:00 PM
    • Q&A
DAY 02(9:00 AM - 5:00 PM)
  • 9:00 AM- 9:15 AM Registration Meet & Greet.
  • 9:15 AM- 10:00 AM
    • Hot water, Chemical, and Ozone Sanitization
  • 10:00 AM- 10:30 AM
    • Source Water Microbial and TOC Destruction in Pretreatment Pharmaceutical Water Systems
  • 10:30 AM- 10:45 AM COFFEE BREAK
  • 10:45 AM- 11:45 AM
    • Non-distillation WFI Options
  • 11:45 AM- 12:30 PM
    • Annex 1 and its Comparison to Compendial Mandates
  • 12:30 PM- 1:30 PM Lunch
  • 1:00 PM- 2:15 PM
    • Myths, Misconceptions, and Realities: The Legacy of Obsolete SOPs and Specifications in Modern Pharmaceutical Water Systems
  • 2:15 PM- 3:00 PM
    • Validation of a Pharmaceutical Water System for the 21st Century
  • 3:00 PM- 3:15 PM COFFEE BREAK
  • 3:15 PM- 4:00 PM
    • Microbial Issues and its Mitigation in Pharmaceutical Waters
  • 4:00 PM- 4:45 PM
    • Sustainability - The Reclaim, Recycle, Reuse and Reduction of Water in Biopharmaceutical Production
  • 4:45 PM- 5:00 PM
    • Q&A
Seminar (Price/Register)
Seminar Fee Includes:
Lunch
AM-PM Tea/Coffee
Seminar Material
Attendance Certificate
$100 Gift Cert for next seminar

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