Liquid Dosage


Bosch Podium Presentation at the 2019 PharmaEd Pre-Filled Syringes Forum

Bosch Packaging Technology is pleased to announce its participation at the 2019 PharmaEd Pre-Filled Syringes Forum, to be held in Boston, MA, on February 27-28, 2019, with a podium presentation by Senior Product Manager Klaus Ullherr. His presentation, titled “Combi Filling – Challenges and Solutions,” will anchor the session on optimization of aseptic filling processes for parenteral containers. The following are a preview of some of the insights Mr. Ullherr will be sharing with the audience: …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


Taking Flexibility to the Next Level? Then Bosch Assembly is Your Choice

Bosch’s Moeller & Devicon factory, based in Denmark, delivers cutting edge assembly technologies for device assembly, labeling, and final packaging to the medtec/pharma industry. Based on highly flexible platforms, and scalable solutions from manual to semi-automatic to fully automatic, Bosch meets the growing needs from the industry. The standard platforms include a newly developed range solution where multiple auto-injector devices can run on the same machine. …more


Product Spotlight: The FXS Combi Filler provides high flexibility when filling individual pre-sterilized components

Pre-sterilized commodities are becoming more and more attractive. The use of pre-sterilized / pre-treated container components has emerged as a promising alternative to conventional primary packaging, adding significant value to streamline pharmaceutical fill / finish. These packaging components eliminate multiple steps in the overall filling process (mainly washing, sterilizing, and preparing containers), thereby helping improve operational efficiencies in compliance to existing regulatory standards. …more


Newly available validation guides for PreVAS products

One of the defining characteristics of the PreVAS single-use product family is the extensive validation work that goes into each product. Validations put the “V” in PreVAS! Bosch PreVAS products are intended to be used for the final fill of mainly parenteral drug products within isolators or other clean room environments; consequently, the products have to comply with the requirements that are given for the manufacturing equipment used for sterile and aseptic processes. …more


Key Takeaways from ISPE’s Third Annual Biopharmaceutical Manufacturing Conference

While last year’s ISPE Biopharmaceutical Manufacturing Conference centered on innovative operational and process development approaches and strategies to speed preparations toward launch readiness, this year’s event, held on December 4-7 in Huntington Beach, CA, focused on the quickly evolving science of biologics manufacturing for new modalities such as those involved in advanced therapeutic medicinal products including CAR-T, cell and gene therapy, and personalized cancer vaccines. Our Bosch Packaging Technology delegates returned from the event with the following key takeaways to report: …more



Mini White Paper: Changeover on a Bosch Packaging Isolator Line

What is “Changeover Time”

ISPE Definition:
The time by which a processing area is cleared of supplies and components used in the manufacture of a previous product and then readied for production of a new product. This often includes parts change over and / or special cleaning to eliminate cross-contamination.

In other words:
Activities and the time needed between two batches …more


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