We are fully committed to the biochemical industry and the pharmaceutical sector. Our core competencies include the passivation of new systems as well as derouging, deblacking, and repassivation of stainless-steel systems.
We offer you full service and bespoke solutions for every type of rouging problem. Quality assurance is just as important to us, which is why we ensure complete documentation every process we conduct.
We specialise in passivation of new systems as well as derouging, deblacking, and repassivation of stainless-steel systems. We offer full service and bespoke solutions for the removal of every type of surface contamination.
We work for a wide range of industries and specialised fields, including:
With our know-how in anodising, colouring techniques, and electropolishing, we can master any challenge. Our state-of-the-art facility in Unterentfelden, Switzerland guarantees fast and professional execution of your projects.
By using the latest technologies, specialised processes, and control systems, we guarantee environmental protection thanks to the reduced use of chemicals as well as recycling.
Our facilities can accommodate parts from 6000 to 7000 mm in length, which enables us to treat even very large workpieces.
We create clarity and assurance at every step of the process. Each phase of your projects is carefully documented with detailed process descriptions.
We exclusively use chemicals that are GMP-compliant and manufactured in Switzerland in an ISO 9000-certified environment.
After every cleaning procedure, we guarantee you the safety of a clean system with no residue.
Our full service includes the correct treatment and disposal of the waste water produced, observing all applicable safety regulations.
A safety concept with precise instructions for work safety, PPE, and emergency measures is drawn up for each specific project.
We guarantee operational success without impairing the system.
We carry out all our technical operations in an SOP-defined, multi-stage, controlled process. We precisely record every measure and every step so that nothing is left to chance. The documentation starts with the initial analysis of the system condition and records all work steps and the use of all chemicals right through to the final inspection.
Transparency and validation
We give you complete transparency – from safe-source, precisely defined chemicals to each individual process parameter like concentration, temperature, and time. All data and procedures are precisely defined, documented, and recorded for you in a manual that supplements your qualification documents once the work has been completed. Our documentation ensures reliable traceability and the compatibility of our work – so that you always have an overview of the condition of your system and can plan maintenance and cleaning accordingly.
We provide you with the following documentation as a standard part of our services:
System condition after treatment (visual assessment, cleanliness, residue measurement, surface roughness, passive condition, etc.)
We guarantee the safety of your system through comprehensive GMP documentation of all cleaning, derouging, and passivation processes. You receive detailed GMP protocols from us, as evidence that the work has been carried out in a manner that can be validated and is transparent.
Our pharma-compliant GMP protocols record every step of the process in detail, monitor compliance with the defined acceptance criteria, and record any deviations. If deviations occur, they are recorded & clarified and appropriate measures taken if necessary.
We provide you with the following protocols and certificates:
With these GMP documents in hand, you can be sure that the maintenance and care of your system is carried out to the highest standards.
