Clean Rooms and HVAC Systems – Qualification, Validation and Monitoring (Medical Device & Pharma)
HVAC Systems and Cleanrooms Professional Certification Course
This intensive two-day program is designed for professionals in the pharmaceutical and medical device industries who work with HVAC systems and cleanrooms.
The course combines essential theory, interactive practice, real-life case studies and practical tools that participants can apply immediately in their daily work.
The training is delivered by industry-recognized experts with extensive hands-on experience and provides participants with an opportunity to discuss questions and challenges from the field.
Course Details
Duration: 2 days | 16 hours of continuing education
Dates and Format:
18.01.2027 | In-person at gstudy Center, Haifa
25.01.2027 | Online
Hours: 09:00–16:00
What You Will Learn
- DQ, IQ, OQ, PQ and Re-Qualification principles
- Particle and microbial monitoring
- Building an effective cleaning and disinfection program
- Disinfectant validation
- Risk management
- Change control
- Practical strategies and tools for daily work
Who Should Attend?
Professionals in the pharmaceutical and medical device industries whose work involves HVAC systems, cleanrooms, facility systems or GMP operations.
Instructor Expertise
The course is delivered by industry-recognized experts with extensive experience in:
- HVAC system design and validation
- Cleanroom qualification and monitoring
- GMP facility operations and maintenance
Prerequisites
A basic understanding of GMP requirements and facility systems is recommended.
Certification and Continuing Education
Participants will receive a Certificate of Participation.
The course provides 16 hours of continuing education credit applicable toward:
- Professional certification maintenance
- Company training requirements
- Regulatory compliance documentation
- Career advancement objectives

Elias Morany
