Micro Filtrations provides timely, comprehensive testing services for cleanrooms and clean devices. Our expertise and equipment will ensure your facility or devices’ continued adherence to the current industry standards, and advise you of preventative measures to maintain compliance. In order to educate our clients on our findings and recommendations, our customers receive an extensive GMP/CFR 211 and ISO-compliant technical report. Our compounding pharmacies receive the report of findings in a format to address USP797 compliance.We pride ourselves on a proactive approach to troubleshooting technical issues, which means that we try to solve problems before they ever occur. Our technicians are among the most certified in the industry, trained to diagnose small issues that could escalate. Request a quote to determine how MFI can help keep your facility in compliance.ASHRAE 110 Fume Hood TestingBiological Safety Cabinets, Fume Hood and Laminar Flow WorkstationsHEPA Filter Leak Integrity TestingDecontaminationAirflow Analysis (Air Volume/Face Velocity Uniformity)Particulate Classification (0.5 & 5.0µm size)Room Air Pattern/Air Exchange ProfileRoom Pressure Differential ProfileData Mapping/Sample Site IdentificationEquipment & Instrument Calibration (with NIST Traceability)Work Area Assessment – Sound/Light/Relative Humidity/TemperatureSurface and Air Sampling – Viable & Non-ViableCompressed Gas, Oil, Moisture SamplingGMP/CFR 211 and ISO compliant technical reportObservations, Corrective Action Recommendations.