Pharmaceutical Facilities

Your Partner in Controlled Environments

Critical Environments

Pharmaceutical environments demand absolute precision. From product integrity to regulatory compliance, every aspect of your building’s HVAC system must perform flawlessly. Our team specializes in designing, maintaining, and optimizing mechanical systems for GMP-regulated and cleanroom-critical facilities, ensuring your operations stay safe, efficient, and compliant.

Being trusted with the responsibility to work within you critical environments is something we take seriously.

Why Pharmaceutical Buildings Trust Us

GMP-Focused Expertise

We understand the strict environmental controls required in pharmaceutical production, such as temperature, humidity, air changes, and pressurization gradients must remain consistent and verifiable. Our service programs are built around Good Manufacturing Practice (GMP) expectations, supported by proper documentation, traceability, and calibration.

Cleanroom Environmental Control

Our technicians are trained in servicing and validating systems supporting:

ISO Class 5–8 cleanrooms
Compounding suites
Sterile packaging areas
R&D laboratories
QA/QC labs

We ensure air quality stability through precise control of HEPA filtration, differential pressures, and room envelope integrity.

Regulatory Compliance

We support the environmental requirements of:

Health Canada & FDA regulations
CSA / ASHRAE cleanroom and ventilation standards
Our service reports and procedures are formatted to align with client SOPs and audit expectations.

Specialized HVAC Services

Preventive & Predictive Maintenance

Pharmaceutical systems cannot afford unexpected downtime. We implement data-driven maintenance programs that include:

AHU and MAU inspections
HEPA and pre-filter lifecycle management
Humidification and dehumidification control
VFD, pump, and motor monitoring
Sensor testing and calibration
Performance trending and analytics

Cleanroom Airflow Balancing & Validation

Our team performs:

Room air change verification
Pressure relationship testing
HEPA leak and integrity testing (PAO / DOP)
Temperature and humidity mapping
Full TAB reports suitable for regulatory audits

Critical System Upgrades

We provide engineered upgrades to ensure your facility meets evolving production needs:

Cleanroom HVAC redesign
Low-temperature dehumidification solutions
High-efficiency filtration retrofits
BMS/EMS integration for audit-ready monitoring
Redundant system installation for 24/7 uptime

Emergency Response

Pharmaceutical processes often run continuously, and environmental drift can halt production. Our technicians are trained for rapid response to:

Loss of critical temperature or humidity
Pressurization failure
Contamination risk events
Mechanical system breakdowns

Your Partner in Controlled Environments

Whether supporting a small compounding lab or a full-scale pharmaceutical manufacturing campus, our mission is to keep your controlled environments operating at peak performance. With deep industry knowledge, certified technicians, and a commitment to quality, we help protect product integrity, ensure compliance, and maintain uninterrupted production.