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SPECIAL EDITIONDAY 3: MIDWEEK AT ACHEMA AND THE BUZZ CONTINUES
ACHEMA is known as the world forum for chemical engineering and the process industry. As movers and shakers gather at Frankfurt am Main from 15–19 June to showcase their innovative technologies, new developments, products, and services, the editors of Pharmaceutical Technology Europe bring you updates from the exhibition floor in this special edition of show daily e-newsletters.
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ACHEMA NEWS
With drug development trends shifting towards personalized medicines, new technologies are needed for the manufacture of these highly sensitive drug products.
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The increasing number of biopharmaceuticals in the development pipeline has created the need for packaging technologies with enhanced safety features, especially for sensitive biologic drugs.
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Schubert-Pharma is featuring the world's first prototype of a packaging machine without an electrical cabinet.
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The high-performance wrap-around labelling machine 132M HC is fully equipped for serialization tasks.
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Pioneering system provides induction sealing integrity analysis for 100% of bottles without packaging line slowdown.
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The Hapa 862, from Hapa AG, is a modular, CMYK/spot-color inkjet printing system for the in-line packaging printing of foils and labels.
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Technologies for serialization and aseptic packaging are being displayed at the show.
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PHARMACEUTICAL MANUFACTURING EXPERTISE: FOCUS ON PACKAGING
ACHEMA is a key event for many industries, including pharma. No doubt the processes involved in pharmaceutical manufacturing have significant impact on the quality and performance of the final drug product. Pharmaceutical Technology Europe has an extensive archive of pharmaceutical manufacturing features and our editors have handpicked some of our top articles to supplement your ACHEMA experience.
Protecting the shelf life of drug products can be achieved passively, actively, or as a combination of the two. The geometry of the blister also plays a role.
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The industry awaits the final revision of USP General Chapter <1207> and the impact it will have on the evaluation of sterile product package integrity.
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