DOCUMENTATION AND QUALIFICATION
Our many years of experience in this field, in particular in the pharmaceuticals industry, set us apart. We deliver pharmaceutical systems with complete qualification documentation, including the design qualification (DQ) – this includes the specification sheet, risk analysis and functional description –, the installation qualification (IQ) and the operation qualification (OQ), as well as the performance qualification (PQ) upon request. The other documentation complies with the pharmaceutical standards and covers the technical documentation as well as the quality assurance documentation. All documentation is available in multiple languages.
We take on the installation and assembly of systems and ring mains on site – both in Austria and around the world – as well as carrying out qualification together with the customer. Our range of services also includes the recalibration of process-relevant measuring equipment: our machine park includes a conductivity measuring instrument, a temperature oven for the calibration of temperature probes, an ultrasound flow meter, a calibrator for pressures up to 700 bar, a measuring device for determining the TOC (the total organic carbon) and a surface roughness measuring device.