Ensuring quality and its consistent improvement are
the two main guidelines of our company.
We ensure the high-quality operation of the
production and implementation of entire projects as well as the safety of
employees, environment and information. This is ensured by means of an
integrated leadership system.
Many different processes take place during the
fabrication of biopharma and Pharmaceutical equipment’s. Several methods are
used to document that the equipment has been equipment designed, fabricated,
inspected, assembled and tested appropriately. These includes,
PMI Testing,
Borescope inspection and video capabilities.
Inspection records, Pre and C-FAT.
All vessels are made out of stainless steel and can
be supplied as stand-alone equipment or as automated process units delivered as
fully-functional modules installed on-site that include: agitators,
homogenisers, metering and regulating technology, control units, valves and
pipe connections. Options for hazardous environments are also available. Our
products are in accordance with the Pressure Equipment Directive, ASME Sec VIII
Div.1 and ASME BPE.