Process Validation with focus on Quality Aspects for the pharmaceutical industry – On-demand

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By Maya Gefen
Engineering & Validation Quality Assurance & Auditing
  • Location: Online/Frontal
  • Duration: 1 Day
  • Starts at: 09:00
  • Language: Hebrew

Process Validation with Focus on Quality Aspects for the Pharmaceutical Industry – On-Demand

This course offers an in-depth overview of process validation in the pharmaceutical industry, following FDA and EMA regulations.

It provides professionals with essential validation knowledge to support regulatory compliance and operational efficiency.

 

Course Details

Availability: On-Demand
Format: On-Site Training

 

What You Will Learn

  • Key regulatory terminology

  • Process validation approaches

  • Quality by Design (QbD) principles

  • Investigation methodologies

  • Continuous process verification

 

Who Should Attend?

Professionals working in:

  • Quality Assurance

  • Regulatory Affairs

  • Manufacturing

  • Development

 

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Maya Gefen

Maya Gefen is a Quality Projects Manager at Gsap with over 25 years of experience in the pharmaceutical industry. She is a recognized expert in cleaning validation, process validation, and compliance with international regulatory requirements. Maya has successfully managed complex quality projects for leading pharmaceutical and medical device companies, including CTS Industries, Rotem Industries, Dr. […]
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