SBM Sterilizer Training Offerings

Bosch-Dampf-Luftgemisch-Sterilisationstechnologie von SBM Schoeller-Bleckmann Medizintechnik

Bosch SBM offers a variety of training in areas such as operator, maintenance, process, calibration, and training customized to your needs. These training offerings are held at the Bosch SBM site in Austria or at your site.

Highlights …more



Inspection technology for all quality and safety requirements

By combining tradition and state-of-the-art developments, Bosch launched two new inspection platforms at Achema 2015: the AIM 3000 and the KHS, which attracted a large audience. “Thanks to the continuous expansion of our inspection portfolio and the cooperation with leading technology suppliers, we can meet all customer and product quality requirements,” says Joachim Baczewski, Global Responsible for Inspection Technology at Bosch Packaging Technology. …more


Low temperature generation of HPW and WFI

The pharmaceutical industry fundamentally requires water in two levels of purity for production: Clean water in PW quality (Purified Water) and water for injection (WFI). The high WFI quality can be produced via technical methods using filtration or distillation processes. However, only distilled water is currently approved for injection purposes in Europe. …more




Product update (with video): Bosch rotary pen assembly machine and new associated labeling unit

At Achema, Bosch Packaging Technology showcased its latest version of the rotary pen assembly machine MRA. Developed by the Bosch subsidiary Moeller & Devicon, the machine is designed to assemble medical devices such as standard four-piece disposable pens or single-shot auto-injectors. These are used, for instance, for diabetes care, the treatment of autoimmune diseases, hormone replacement therapies or emergency medicine. Because the majority of pens and auto-injectors need to be further labelled, Moeller & Devicon has recently launched a labeling unit which stands in line with the assembly machine. …more


The right implementation of an EU-Guideline with solutions by Bosch

The purpose of the guideline 2011/62/EU is the standardization of safety features, in order to control authenticity and in order to identify packaging in the EU. Therefore, the pharmaceutical industry will have to manage the resulting challenges: As of the first quarter 2018 all prescription and some over-the-counter medicines will have to inlcude a 2D Data Matrix Code and a tamper evident closure. …more




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