Posts Tagged ‘Trainings/Seminars’

Inspiring insights at the PDA in Mainz and Gothenburg

October 9 and 10, 2019, the training for “Best Practices for Glass Primary Containers” of the Parenteral Drug Association (PDA) in Mainz entered its third round. After the success of the courses in the past years, participants could look forward to interesting and practice-oriented lectures and an experienced team of trainers this year. …more


Cluster merger strengthens competitiveness

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



Discover the world of pharma filling technologies

Bosch has been inviting to its Pharmatag in Crailsheim, Germany, and giving new impetus to the industry for more than 40 years. The traditional event is about to take place again from May 21 to 22, 2019, this time under the motto “Expertise for the perfect flow”. …more




Promising talents to shape the pharma world

From January 29 to 31, the 6th All-Russian Student Pharmaceutical Olympiad was held in Nizhny Novgorod. Next to many pharmaceutical companies, Bosch Packaging Technology was the only equipment supplier to support this event. “As a first-time partner to the Pharmaceutical Olympiad, this event was a great opportunity to interact with promising talents,” says Ralf Schmied, Vice President Product Group Pharma Solid at Bosch Packaging Technology. …more


Requalification – GMP-requirements for the pharmaceutical industry are valid worldwide

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


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