The implementation of EU GMP Annex 1, which sets strict requirements for the production of sterile medicines, presents new challenges for pharmaceutical companies. In the foreseeable future, Ralf Wagner, Sales Director for the DACH region, Portugal and Spain at Optima Pharma, believes that glove int…
The new CO₂ cooling technology in environmental simulation not only meets the requirements of the EU F-Gas Regulation for single-stage refrigeration systems but also accelerates processes in test laboratories. With the extended temperature range of the new test chambers reaching −50°C, changes…
Proton exchange membranes (PEM) are one of the most promising technologies for the production of green hydrogen by electrolysis. To reduce the material and manufacturing costs for PEM electrolyzers, the Fraunhofer Institute for Solar Energy Systems ISE is researching scalable production processes. N…
Ruland Engineering & Consulting GmbH has been planning and building process systems for the production of liquid products since 2000. What began with just seven employees has developed into an international company with 320 employees and 5 locations. Ruland stands for process plants with the hig…
Innovation ist eine fest in der Unternehmenskultur verankerte Leitlinie des Ventilatoren- und Motorenherstellers ebm-papst mit Sitz in Mulfingen. Nun wurde die Innovationskraft des Technologieführers bereits zum dritten Mal mit dem TOP 100-Award ausgezeichnet. Der Wettbewerb ehrt besonders innovati…
The manufacture of mostly sensitive, highly complex and/or high-quality cleanroom products in a controlled environment that is as clean as possible, requires specific principles to ensure the desired product properties. After all, cleanroom products are subject to the most stringent requirements.
By…
Choosing the right containment system—isolators, biosafety cabinets (BSCs), or restricted access barrier systems (RABS)—impacts sterility, compliance, and efficiency in aseptic manufacturing.
Maintaining strict sterility in pharmaceutical manufacturing is non-negotiable. Regulatory frameworks such as A…
– RMA assembly solution for pens and autoinjectors recognized for user-friendliness and seamless processes.
– Design simplifies operations and enables flexible production.
– Long-term value for pharmaceutical manufacturers of, for example, antidiabetics and weight-control products.
Syntegon has received t…
How do lithium-ion batteries for electric vehicles react to heat, cold and rapidly fluctuating temperatures? This is tested repeatedly during their development and production in order to guarantee the safety of the energy storage systems. Weiss Technik has provided 22 test chambers for the VW Batter…
With the implementation of the EU GMP Annex 1 ("Manufacture of Sterile Medicinal Products"), pharmaceutical companies are facing new challenges, particularly in the fill-and-finish processes—the filling and final processing of medicinal products. Annex 1 introduces expanded requirements for both e…
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