In pharmaceutical production, the quality of process and supply gases is a critical factor for product safety and regulatory compliance. Particulate contamination in gases can impair sterile processes and must therefore be reliably evaluated as part of cleanroom qualification and ongoing monitoring.
The particle-in-gas measurement method in Moqlero was developed specifically for pharmaceutical cleanroom applications. It enables the digital recording and structured evaluation of discontinuous measurements to detect particulate contamination in process and supply gases. It thus supports qualifications, re-certifications, and the assessment of the suitability of gases for use in critical areas.
All measurement data is processed completely digitally and documented in an audit-proof manner. The application automatically generates audit-ready reports that meet the requirements of regulated pharmaceutical environments and enable a traceable assessment of gas purity.
As part of the Moqlero platform, the particle-in-gas measurement becomes a standardized, efficient, and audit-ready process for the control of critical media in the pharmaceutical industry.
Make the purity of your supply gases transparent and regulatorily secure – with the digital particle-in-gas measurement in Moqlero.