SECTOR 01 · PHARMACEUTICAL
Pharmaceutical Clean Room HVAC Engineering
cGMP Schedule M, ISO Class 5–8 cleanroom HVAC, pressure cascade control, and HEPA air handling systems for pharmaceutical formulation & API plants in Gujarat.
Key Air Engineering Focus Areas
Custom HVAC systems designed specifically for high operational performance, environmental compliance, and worker thermal comfort.
Granulation & Compression Bays
Positive pressure air lock management preventing cross-contamination of active pharmaceutical ingredients (APIs).
cGMP Schedule MISO Class 7/8Sterile Injectable Filling
ISO Class 5 laminar airflow workstation units with gel-seal H14 HEPA filters and continuous particle monitoring ports.
ISO Class 5Sterile FillingStability Chambers & Warehousing
Tight relative humidity control (25°C ± 2°C / 60% RH ± 5%) for active sample stability testing & bulk raw material storage.
Dehumidification24/7 LoggingRegulatory Compliance & Engineering Standards
Schedule M / WHOMandatory Air Change Rates & Room Differential Pressure.
ISO 14644-1Particle Count Classification & Recovery Tests.
US FDA Audit ReadyComplete Validation Dossiers (DQ/IQ/OQ/PQ).
Zero Leakage DuctsIn-house fabricated low-leakage GI ductwork.
INDUSTRY FAQs
Frequently Asked Questions
What air change rate (ACPH) is required for ISO Class 7 cleanrooms?
ISO Class 7 cleanrooms typically require 30 to 60 air changes per hour (ACPH) with terminal H14 HEPA filtration to maintain particulate limits under operational conditions.
Do you manufacture zero-leakage ductwork for pharma plants in-house?
Yes, all our ductwork is manufactured in our Vatva/Mehmdavad factory using CNC plasma cutters and lockformers to guarantee SMACNA Class A seal standards.
Need a Custom HVAC Design for Your Facility?
Consult with our senior application engineers in Vatva, Ahmedabad today.