Water System Validation in Pharmaceutical Industry

This webinar will discuss the FDA requirements for design, validation and monitoring of pharmaceutical water systems. There are many different types of pharmaceutical waters and each must be fit for its intended use. Pharma water must be controlled for impurities. Pharma water systems must be designed, validated and monitored to ensure that the water produced meets specifications around the clock. Learn common pitfalls with water system design and use and how to avoid them. Get your pharma water questions answered in this webinar.

Areas Covered in the Session :

  • Types of Water Systems used in the Pharmaceutical Industry
  • Regulations Guiding Pharmaceutical Water
  • Current USP <1213> Pharmaceutical Water System
  • How pharmaceutical grade water is produced
  • Validating a newly commissioned Water System
  • Water System Validation by Logic
  • Establishing procedures for maintaining the water system during its lifecycle
  • Post Validation Testing
  • Pharmaceutical Water Failure
  • Presenting the results to auditors

Who Should Attend:

  • Quality Assurance Departments
  • Quality System Auditors
  • Manufacturing Departments
  • Regulatory Affairs Departments
  • Research and Development Departments
  • Engineering Departments
  • Compliance Departments
  • Microbiology Analysts and Technicians
  • Lab Personnel
  • Logistics
  • Consultants

FDB3525

HitendraKumar Shah

HitendraKumar Shah is a renowned Quality oriented professional with over 20 years of experience in Quality Assurance and Quality Control. During this period, he has been actively involved in process control, Finished product release, Investigations, product recalls and other quality notifications. He has helped numerous companies in ensuring CAPA implementation & effectiveness, Quality system review and reporting, Supplier audit, GMP training, risk assessment and validation activities. His Key Competencies are but not limited to Quality Compliance, Vendor Audit, data integrity, Risk assessment, Qualification & validation, Review and finalization of technical agreements. He is a popular figure on social media for his effective and easily understandable training bites.

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  • Login Information with Password to join the session, 24 hours prior to the webinar
  • Presentation Handout in .pdf format
  • Presentation from the Speaker
  • Feedback form
  • Certificate of Attendance
  • Recording access Information with Password to view the webinar, will be sent 24 hours after the completion of the Live webinar.
  • Presentation Handout in .pdf format
  • Certificate of Attendance