Services

Technical scopes built for performance & compliance

Pharma Cleanrooms
Process Engineering
HVAC
HVAC Design & Engineering
Validation
Calibration & Metrology
General Contracting

Pharmaceutical Cleanrooms

  • Concept → Design → Build-out for ISO 7/8 suites
  • Commissioning, qualification & validation packages (DQ/IQ/OQ/PQ)
  • Environmental monitoring setup; CAPA & deviation handling
  • Change control and turnover documentation

Process Engineering

  • URS/FRS development aligned to GMP workflows
  • CQV planning; equipment qualification protocols
  • Material & personnel flow design; risk assessments (FMEA)
  • Utilities: compressed air, HVAC, power distribution considerations

HVAC

  • Preventive maintenance programs with SOPs and logbooks
  • Installations & retrofits; VFD, controls, and air-side upgrades
  • Cleanroom-grade air balancing; HEPA integrity and filtration validation
  • Emergency response and uptime improvements

HVAC Design & Engineering

Comprehensive HVAC Design & Engineering Solutions

  • Complete design capabilities aligned with ASHRAE standards and GMP best practices.
  • Custom solutions for pharmaceutical, industrial, and commercial environments.
  • End-to-end delivery from concept through commissioning—airflow, zoning, filtration, and controls meticulously engineered for reliability and efficiency.

As-Built Documentation & Traceability

  • Comprehensive as-built drawings capturing the final configuration of HVAC and mechanical systems.
  • Reflects all field adjustments and design evolutions for accurate reference, inspection, and ongoing facility management.

Load Calculations & System Optimization

  • Detailed load calculations performed per ASHRAE guidelines for proper sizing and system balance.
  • Analysis of envelope, occupancy, equipment, insulation, and ambient conditions to define precise heating, cooling, and air distribution requirements.
  • Foundation for efficient, compliant, high-performance systems that meet **GMP cleanroom** standards and long-term goals.

Validation

  • System/equipment qualification (DQ/IQ/OQ/PQ)
  • Validation protocols, reports, and traceability
  • Data integrity and change control
  • Audit readiness support

Calibration & Metrology

  • ISO/NIST traceable calibration and certificates
  • Schedules & reminders; instrument asset registry
  • Deviation documentation and corrective actions
  • On-site or lab partnerships for specialty equipment

General Contracting

  • HVAC, Electrical, and Plumbing coordination
  • Tenant improvements & office build-outs
  • Phased renovations for live facilities
  • Permitting support and inspections coordination