Frequently Asked Questions
Clear answers regarding cleanroom designs, ISO classes, HVAC filters, and validation timelines.
FAQ Categories
General Inquiries
All our structural panels, airlocks, and HVAC validation metrics adhere strictly to ISO 14644-1 parameters, WHO GMP guidelines, EU GMP Class A/B/C/D layouts, and US FDA audit criteria.
We serve pharmaceutical formulations, biotech containment laboratories, hospitals (ICUs and modular OTs), food packaging plants, and static-free electronics/semiconductor clean rooms.
Documentation Services
Our qualification binder contains a validation matrix, DQ/IQ/OQ/PQ protocols, calibration logs, air balancing details, and certified reports suitable for submission to inspectors.