Liquid Dosage in asia

Ensure your Compliance of Good Distribution Practice (GDP)

Quality compliance of active substances/medicinal products from storage to marketing must be ensured. In Addition to GMP (Good Manufacturing Practice), GDP specifies the guidelines for the distribution process, which ensures consistency of the high quality level a manufactured pharmaceutical product has to arrive at the consumer. …more


Interesting Insights at the Pharma Congress Production & Technology 2019

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





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


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




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