Cleanroom and controlled-environment certification built around the Canadian regulatory standards your facility is audited to — NAPRA Model Standards for sterile and non-sterile compounding pharmacies, Health Canada Annex 1 (GUI-0119 v2, May 2024) for GMP manufacturing, and PHAC Canadian Biosafety Standard for CL2/CL3 containment laboratories, with ISO 14644-1 classification and USP <797>/<800> compliance where applicable. Compounding pharmacies, hazardous compounding rooms, GMP manufacturing cleanrooms, and biocontainment laboratories each have meaningfully different engineering and testing requirements; CAM certifies all four.

We install, certify, and service the full range of laboratory and critical equipment — biological safety cabinets, fume hoods, laminar flow workstations, containment isolators (CACIs), containment ventilated enclosures (CVEs), powder containment hoods, refrigerators, freezers, incubators, ovens, and analytical balances. CAM performs new equipment installation (uncrate, position, level, secure — with sheet metal and HVAC trades coordinated and billed through CAM as a single point of contact), field certification and recertification, calibration verification, repairs, and preventative maintenance. All work is performed on-site by NSF-accredited, CETA-Registered technicians and documented to applicable regulatory and industry standards — including the NSF/ANSI 49 Annex N-5 field certification battery, CSA Z316.5 for fume hoods, CETA Application Guides (CAG-002 for isolators, CAG-003 for sterile compounding facilities), and the equipment maintenance & calibration requirements set out in NAPRA and Health Canada GMP.

Field certification, environmental monitoring, and documentation services for sterile compounding pharmacies, hazardous drug compounding facilities, pharmaceutical manufacturers, biotechnology facilities, and radiopharmaceutical environments. We deliver the on-site testing data and certification reports your QA team, validation consultancy, or compliance lead uses to maintain programs aligned with NAPRA Model Standards, USP <797>, USP <800>, Health Canada GMP (GUI-0001), Health Canada Annex 1 (GUI-0119), and Good Production Practices (GPP).

CAM is your field certification and monitoring vendor. We work directly with pharmacy directors and QA leads — and in subcontracted partnerships with validation consultancies and engineering firms managing GMP compliance for their clients. We don't author validation protocols or run formal IQ/OQ programs. We deliver the on-site testing, sampling, and documentation those programs depend on.

NAPRA Model Standards-compliant environmental monitoring for sterile compounding pharmacies, hospital pharmacy services, GMP facilities, and controlled environments. Viable air & surface sampling, non-viable particle counting, genus-level identification of growth, and trend analysis — performed every six months under documented monitoring schedules, with additional sampling triggered by new installations, repairs, or contamination investigations. From program design through ongoing execution and excursion response, CAM delivers the data your facility needs to maintain audit readiness with provincial regulatory authorities.

Clean Air Monitoring works with trusted analytical laboratory partners to deliver coordinated testing programs — sample collection, analysis coordination, interpretation, reporting, and investigation support.

Specialized contamination assessment and forensic support services for law enforcement, healthcare, research, industrial, and controlled-access environments requiring regulated contamination verification, documentation, and remediation support.

Planning a new cleanroom? Installing biosafety cabinets, laminar flow workstations, fume hoods, or modular cleanroom systems? Expanding capacity? Upgrading containment systems? Decommissioning equipment or facilities? Clean Air Monitoring supports every transition point in your facility's lifecycle.