Qualification

There is movement in industrial hygiene and safety. SKAN has developed a robot-assisted test procedure especially for containment tests for the development and maintenance of fume cupboards.

Rooms are decontaminated using common processes fogging or aerosolization. This gently and reliably reduces germ contamination on surfaces, filters, inserted and removed materials and equipment.

For added protection of pharmaceutical and regulated manufacturing operations, the filters must pass regular HEPA filter integrity tests.

SKAN has many years of experience in the control of regulated production areas and therefore offers a proven microbiological monitoring.

SKAN offers a wide range of air and liquid particle counters, as well as the best advice and service for every requirement.

Good Manufacturing Practice (GMP) requires both qualification (IQ, OQ) and requalification (ReQ) of pharmaceutical equipment.

The special requirements of cleanrooms demand well documented tests as proof of optimal conditions and compliance with all standards and regulations.

Thanks to decades of experience in repair and maintenance, SKANs specialists recognize every problem directly and know the right solution.

SKAN offers regular controls, preventive maintenance, recalibrations and re-qualifications for all forms of equipment and systems.

The validated fumigation process with hydrogen peroxide gives an excellent decontamination result and thus a safe plant in a very short time.

At SKAN, the installation of a system not only includes the delivery, but also everything from assembly to commissioning.

Through active exchange with customers from various industries, SKAN has an up-to-date knowledge base covering most laboratory fields. The SKAN Academy teaches this knowledge base objectively and with training certificates; the contents are provided as learning material.