Cleaning Validation Seminar for the Pharmaceuticals Industry

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Date: Nov 10, 2026
By Iris Shamir
Registration
Quality Assurance & Auditing Engineering & Validation
  • Location: Online + Frontal
  • Duration: 1 Day
  • Starts at: 09:00
  • Language: Hebrew

Cleaning Validation Seminar for the Pharmaceutical Industry

The seminar reviews the regulatory requirements and guidelines throughout the cleaning validation lifecycle.

Participants will learn from examples of regulatory authorities’ observations, explore how to avoid common mistakes and take part in practical case study exercises.

 

Course Details

Duration: 1 day
Date: 10.11.2026
Hours: 09:00–17:00
Location: gstudy Center, Haifa

 

What You Will Learn

  • Regulatory requirements
  • The cleaning validation lifecycle
  • Calculating cleaning limits
  • Risk management for worst-case selection
  • Validation of the analytical method
  • Microbiological considerations in cleaning
  • Cleaning validation for biotechnological products
  • Examples of observations from regulatory authorities
  • Avoiding common mistakes
  • Case study practice
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iris-shamir

Iris Shamir

Pharmaceutical Quality and Regulatory Executive with more than 25 years of experience in Quality Assurance, Compliance, Quality Control and Regulatory Affairs across the pharmaceutical, biotechnology and medical device industries. Former GMP Inspector at the Israeli Ministry of Health with extensive experience in manufacturing oversight, regulatory inspections and quality system transformation. Specialized in GMP, GxP, FDA […]
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