
Solution
Why Choose Us?
Complying with International Standards
Products comply with ISO, EN 779, and EN 1822 standards, meeting GMP and EU GMP requirements for pharmaceutical and healthcare applications.
Project-Specific Design
No one-size-fits-all solutions — each cleanroom is individually analyzed and designed to meet specific project requirements.
Fast Implementation & On-Time Delivery
Committed to responding within 24 hours, with installation and commissioning completed on schedule.
Long-Term Support
Regular maintenance, upgrade consultation, and component replacement support throughout the system’s lifecycle.
Solution
- H13–U17 HEPA / ULPA Filters
- Fan Filter Unit (FFU) and Terminal Housing
- AirShower, PassBox, LamiHosp
- Positive / Negative Pressure Control System.
- Bag-In Bag-Out for Hazardous Environments
- Consulting on Acceptance Testing in Accordance with ISO 16980
Frequently Asked Questions (FAQs)
Does Air Filtech consult on cleanroom design from the start?
Yes — our technical team analyses requirements, proposes the appropriate ISO level and designs the system for each specific project.
How long does it take to implement a cleanroom system?
Depending on scale, typically 2–8 weeks from order confirmation to acceptance.
Does Air Filtech provide post-installation maintenance?
Yes — we offer periodic maintenance contracts, component replacement and technical support throughout the system lifecycle.
Do products meet GMP standards?
All cleanroom filters are certified to EN 1822, ISO 29463 and comply with GMP / EU GMP requirements.