Our clean room ventilation services cater to pharmaceutical, food manufacturing, and laboratory facilities. We design and implement controlled airflow systems to maintain sterile conditions and meet regulatory requirements.
Engineering design of HVAC systems for ISO Class 5–8 and GMP Grade A–D clean rooms, specifying air change rates, filtration, pressurization, and temperature/humidity control.
Supply and installation of Fan Filter Units (FFUs) with ULPA or H14 HEPA filters to create unidirectional laminar flow in clean manufacturing areas.
Design and validation of positive and negative pressure cascades between clean room zones to prevent cross-contamination and maintain classification boundaries.
IQ/OQ/PQ validation of clean room HVAC systems including particle counting, air velocity surveys, recovery tests, and containment leak testing.
GMP & ISO Compliance: NILRIC clean room systems are designed to meet GMP Annex 1, ISO 14644, and FDA 21 CFR Part 11 regulatory requirements for pharmaceutical and laboratory environments.
Energy-Efficient Design: Advanced variable air volume (VAV) control and EC motor FFUs significantly reduce the energy cost of maintaining clean room classification 24/7.
Full Project Lifecycle Support: From initial concept design through installation, qualification, and ongoing maintenance, NILRIC provides complete clean room lifecycle management.
Rapid Contamination Recovery: Properly designed clean room HVAC systems recover to required particulate classification quickly after door openings or process disturbances, minimizing downtime.
Ready to get started? Contact us today or call +255 796 009 316.