Industry Focus

Pharmaceutical Manufacturing

GMP-compliant climate control with precise humidity and particulate management. Specialized execution for Houston's most demanding environments.

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Pharmaceutical manufacturing facilities require arguably the most stringent air quality and climate control standards of any industry. We provide HVAC solutions that maintain ISO-certified cleanroom environments, ensuring product integrity and regulatory compliance. Our systems are designed to control particulate count, temperature, humidity, and differential pressure with absolute precision.

Our Process

We work closely with process engineers and validation teams to design HVAC systems that integrate seamlessly with manufacturing workflows. Our installation process includes rigorous protocol adherence to maintain cleanliness standards throughout construction.

Key Benefits

Contamination Control: Advanced filtration (HEPA/ULPA) and pressure cascading to prevent cross-contamination.
Regulatory Compliance: Systems designed to meet FDA cGMP, EU GMP, and ISO 14644 standards.
Validation Support: Comprehensive documentation and testing support for IQ/OQ/PQ validation processes.

What's Included

Cleanroom HVAC Design & Installation

HEPA/ULPA Filtration Systems

Cascading Pressure Controls

Desiccant Dehumidification

Process Cooling & Chillers

Validation Documentation Support

Overview

We engineer air. For pharmaceutical clients, this means delivering environments where chemistry and biology can be manipulated safely and reliably, protecting both the product and the personnel.

Compliance & Standards

All installations are fully compliant with FDA 21 CFR Part 210/211, ISO 14644 cleanroom standards, and ISPE Good Practice Guides.

Frequently Asked Questions

Do you have experience with GMP facilities?

Yes, our team is trained in Good Manufacturing Practices (GMP) and understands the documentation and cleanliness rigor required for pharmaceutical projects.

How do you handle critical shutdowns?

We plan shutdowns with military precision, often executing critical tie-ins during scheduled plant maintenance windows to minimize production impact.

Ready to Discuss Your Project?

Get a detailed estimate for pharmaceutical manufacturing. No obligation, just expert advice.

Typical Project Timeline

Consultation & Load Analysis

Week 1-2

Site survey, load calc, and equipment selection.

Proposal & Permitting

Week 3

Detailed quote, contract signing, and city permit filing.

Mobilization & Install

Week 4-6

Equipment delivery, crane lift, installation, and ductwork.

Commissioning

Week 7

System startup, balancing, testing, and handover.

Efficiency Standards (2025)

System Type	Min. SEER2 / IEER	Target
Split System (<65k BTU)	14.3 SEER2	16+ SEER2
Rooftop Unit (Packaged)	14.8 IEER	18+ IEER
VRF / VRV Systems	18.0 IEER	22+ IEER
Water-Cooled Chiller	0.58 kW/ton	0.52 kW/ton

Higher efficiency ratings often qualify for CenterPoint Energy rebates and tax incentives.