Validation and Monitoring of HVAC Systems and Clean Rooms Training

Medical devices industry Gsap
Gstudy > Courses and seminars > Validation and Monitoring of HVAC Systems and Clean Rooms Training

Dec 16, 2025

By Jose (Yossi) Chvaicer, M.Sc. & Meir Podriadchik Paz

Cycle 4

Engineering & Validation

Quality Assurance

Location: Frontal

Starts at: 09:00

Duration: 2 Days

Language: Hebrew

Professional Certification Course | 2-Day Intensive Program

 

Take Your Cleanroom & HVAC Expertise to the Next Level! 

 

Working in pharma or medical devices? If HVAC systems or cleanrooms are part of your daily reality, this course is built for you.

 

  • ✅ A practical training program packed with real-life case studies and tools you can apply immediately.
  • ✅ Delivered by top industry experts with decades of hands-on experience.
  • ✅ A perfect blend of essential theory, interactive practice, and proven strategies.
  • ✅ Bring your toughest questions from the field – get clear, tailored answers.

 

Why Join?

  • ✅ Master DQ, IQ, OQ, PQ & Re-Qualification principles
  • ✅ Gain confidence in particle & microbial monitoring
  • ✅ Build an effective cleaning & disinfection program (incl. disinfectant validation)
  • ✅ Strengthen your risk management & change control skills
  • ✅ Walk away with actionable tools to improve your daily work

 

  • 📌 Dates: December 3 & 10, 2025 | 09:00–16:00
  • 📌 Location: Gstudy Training Center, MATAM Haifa
  • 🎓 Includes a Certificate of Participation
  • 👉 Seats are limited – secure your spot today!

 

 

Instructors Expertise

Course delivered by industry-recognized experts with extensive experience in:

  • HVAC system design and validation
  • Clean room qualification and monitoring
  • GMP facility operations and maintenance

 

 

 

Registration Information

  • Early Bird Pricing: Available for registrations 30 days in advance
  • Group Discounts: Available for 3+ participants from same organization
  • Custom Corporate Training: Available for 8+ participants
  • Prerequisites: Basic understanding of GMP requirements and facility systems recommended

 

Continuing Education

This course provides 16 hours of continuing education credit applicable toward:

  • Professional certification maintenance
  • Company training requirements
  • Regulatory compliance documentation
  • Career advancement objectives

 

  • About Jose (Yossi) Chvaicer, M.Sc.

    Mr. Jose Chvaicer graduated in Mechanical Engineering from the State University of Rio de Janeiro, Brazil, and he has a Master’s Degree in Industrial and Management Eng. from the Technion – Israel Institute of Technology, Haifa, Israel. Jose holds a lead auditor certificate from the IIS (ISO9001, ISO13458).He has over 25 years of international experience in the Pharmaceutical Industry. While...
  • About Meir Podriadchik Paz

    Mr. Meir Podriadčík Paz holds a Bachelor's degree in Animal Sciences from the Hebrew University of Jerusalem and a Master's degree in Business Administration with specialization in Bio-Medical Systems Management (Bio-M.B.A) from the Academic Track at the College of Management. Meir is a Quality Assurance (QA) expert with over 10 years of experience in the pharmaceutical and medical device industries,...

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Registration Information

Early Bird Discount: 30 days in advance
Group Rates: Available for 3+ participants
Corporate Training: Custom programs for 8+ participants

Contact: Gstudy@gsap.co.il

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