How to transfer products into barrier systems

There are many things to consider when transferring products and materials into barrier systems. It begins with categorizing the pharmaceutical product and defining the aseptic environment. How is my product categorized? What processes and procedures are commonly used? Which room classifications are available? These and many other questions are a first baseline to start with.

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Product Manager Matthias Angelmaier at the PDA Taiwan and 3rd Annual Aseptic Processing Summit in Vienna

Focusing on the impact of digitization on pharmaceuticals, manufacturing and patient care the “PDA Drug Delivery of Injectables Conference” took place in Taipei, Taiwan from November 12 to 13, 2019. One of the goals of this conference was to answer the following questions: How can primary packaging and the fill-finish process interact? Which devices such as pens, auto-injectors and wearables with electronic functions are available on the market? What is the current status of digital technologies in an aseptic environment? And what are the advantages for the patient? …more


Risk management: must-have for any pharmaceutical company

Quality Risk Management (QRM) is a systematic process for assessing, controlling, communicating and reviewing risks that affect the quality of a medicinal product. An efficiently implemented quality risk management system (QRM) ensures the quality of products throughout the entire life cycles and is an enabler of the Pharmaceutical Quality System (PQS). …more


Xelum R&D on world tour

Bosch Packaging Technology’s Xelum R&D for the continuous production of oral solid dosage (OSD) forms holds substantial potential: since it was first introduced to selected customers in 2018, the compact, innovative machine has attracted considerable interest. …more





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