We offer a comprehensive service that combines technical consulting, specialized training, and expert audits to help you strengthen contamination control and optimize your production processes.
Technical Consulting:
We provide expert support to implement and enhance technical cleanliness processes, define acceptance criteria, and resolve deviations with a data‑driven approach.Training:
We design structured training programs aligned with industry standards, ensuring formal instruction that can be directly applied to the industrial environment.Technical Audit:
We conduct process and technical cleanliness audits to assess compliance with standards and best practices, identify risks, and detect opportunities for improvement.“These tests make it possible to investigate the origin and causes of defects in components and materials through characterization techniques and damage analysis. They are essential for problem‑solving, preventing recurring failures, and providing technical support for decision‑making.
Cavitation measurement makes it possible to assess the actual performance of ultrasonic equipment used in cleaning processes. These tests enable the characterization, comparison, and optimization of processes, helping to refine process parameters and ensure cleaning repeatability and effectiveness under real operating conditions.
Environmental contamination measurement makes it possible to assess the level of particles present in the manufacturing environment and within the process itself, helping to identify potential sources of contamination. It is an essential tool for ensuring process control, preventing defects, and optimizing production conditions, thereby securing more stable and reliable environments.
These inspections are aimed at assessing technical cleanliness in medical devices, taking into account the specific requirements of this sector. They allow verifying the effectiveness of cleaning processes, supporting process validation, and ensuring compliance with applicable standards in regulated environments.
These inspections enable the assessment of the technical cleanliness level of components and systems in accordance with VDA 19.1, ISO 16232, as well as customer-specific standards, by verifying the level of residual particle contamination in the product, supporting the validation of cleaning processes and ensuring compliance with industrial and customer requirements.
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