Validated, Reliable, Efficient

The Smarter Way to Manage Clean Rooms

Moqlero isn’t just a tool — it’s your competitive edge.
Unlike systems designed for 24/7 sensor feeds, our platform is purpose-built for discontinuous clean room monitoring, classification, and recertification. Designed with precision, scalability, and compliance in mind, it connects the physical world of clean rooms with cutting-edge digitalization. As the central backbone of your contamination-controlled environment, Moqlero helps you drive efficiency, ensure quality, and accelerate decision-making.

Ready to future-proof your clean room? Discover how Moqlero delivers measurable results — fast.

Process and Methodology

From Setup to Success: An Overview

Not Another Continuous Monitoring Tool.

Continuous, sensor-driven monitoring solutions are excessive for many clean environments, both in terms of cost and complexity. Recognizing this gap, Moqlero is engineered to meet the exacting demands for automation in discontinuous monitoring environments. It digitizes manual, scheduled, and on demand ad-hoc measurements, avoiding data overload and instead focusing on timely, and targeted measurements.
Its core area of application is executing scheduled and event based monitoring, classification and recertification of clean room environments.

Automated control of particle counters and evaluation of measurement results are naturally included.

Central Overview of SAP workorders for discontinuous particle and air measurements

Automated Workflows 1.0

Built-In Deviation Management

In the event of a detected deviation, such as defective filters, the system immediately notifies the responsible personnel via automated alert functions. The responsible person is required to evaluate the situation without delay and, if necessary, initiate corrective actions.
Using electronic signature functionality within the system, the responsible person can directly assign and approve an immediate repeat measurement after the completion of the repair work, ensuring full traceability and compliance with GMP requirements. All activities, including deviation detection, notification, corrective measures, and the assignment of the repeat measurement, are documented within the electronic system and linked to the corresponding work order.

Such guided resolution paths not only ensure regulatory compliance but also boost confidence in decision-making during critical situations.

Automated Workflows 2.0

Integrated Change Procedures

A structured and intuitive workflow is provided to easily enable or modify key master data, such as particle measurements. This flexibility allows teams to adapt quickly to evolving operational or regulatory demands—keeping all processes efficient, consistent, and fully under control.

Business Values

Clean Room Control That Pays Off

We turn complexity into clarity, helping you stay ahead through intelligent automation, traceable processes, and seamless evaluations. Provided benefits include:

Quality Improvement	Efficiency Boost
Cleanroom Audit: Prepared. Safe. Complete.	Stress-Free: No tedious searching, verified data integrity, full traceability, secure documentation
High Degree of Automation in Measurements	Minimization of Measurement Effort
Uniform, Paperless Documentation	Automated Report Generation
Deviation Handling Fast and Secure	Automated Evaluation and Handling of Results
Measurement tasks Compliant and Error-Free	Clear, Digitized and Predefined Information Paths

Documents and Reliability

Computer System Validation

We provide all the documentation you need for smooth and complete CSV — clearly structured, comprehensive, and ready for use.
This includes comprehensive manuals, clearly defined functional specifications, and detailed test specifications. The materials are structured to align with industry best practices and facilitate efficient qualification of our software within GxP-regulated environments.