To meet the requirements of complex global pharmaceutical markets, companies not only need innovative machines but also qualified personnel and efficient processes. We provide everything from a single source. …more
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
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
(Russian Version below)
At Pharmtech in Moscow, visitors to booth B6021 (pavillion 2, hall 8) are in for a local premiere, some exciting action, an inspiring talk, as well as a few new and familiar faces.
Medicinal products differentiate from other products as quality deficiencies of medicinal products may result in serious consequences for consumers. Therefore, guidelines for Good Manufacturing Practice (GMP) are obligatory for pharmaceutical manufacturers in Europe. But what does a GMP certificate mean and who can obtain it?
In 2020, Bosch Packaging Technology will reinvent itself. With the planned acquisition by CVC Capital, the processing and packaging technology division will be separated from the Bosch Group and will operate as a medium-sized enterprise. This fits in perfectly with a new and exciting market development: the planned merger of Packaging Valley e.V. (PV) and Packaging Excellence Region Stuttgart e.V. (PEC) into a large joint network. …more
Market trends towards smaller batches, higher quality products and online quality control require production solutions that ensure stable, monitored processes to achieve high dosing accuracy, high yield and high OEE. Do these requirements look familiar to you?
From April 9th to 10th, the annual Pharma Congress Production & Technology will again take place in Düsseldorf. For years, this event has been known as a meeting place for the industry and is now also valued as an international forum far beyond its borders. …more
The initial achieved qualification status has to be maintained durably. For this purpose, relevant influencing factors on General Manufacturing Process (GMP) have to be checked periodically. The regulatory requirement of requalification is mandatory worldwide. Prominent superordinate regulations are the GMP guidelines of the US and the EU as well as the guidelines of PIC/S. …more
