Hot-Melt Extrusion Progress Continues
Presenters at a pharmaceutical extrusion seminar discussed formulating drugs produced using hot-melt extrusion.
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Now Online To read about how the EU and US are strengthening the supply chain for pharmaceutical ingredients, read the online article from the July issue of Pharmaceutical Technology.
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Solving Common Problems in Warehouse Management
Warehouse layout and personnel training are crucial to successfully implementing a warehouse management solution.
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Fette Compacting America Inc
Single rotary tablet press offers fastest changeover time in its class
A single rotary tablet press that can be fitted with up to 51 stations,
 Fette America's FE35 Tablet Presscan produce up to 367,000 tablets per hour. Complementing this unprecedented level of productivity is the fastest changeover time in its class. The FE35 is clad in easily-detachable, FDA-certified high-performance polymer panels and offers 360-degree access. |
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Bosch
Need some expert advice? Check out the Expertise Series on our blog for tips and tricks to get the most out of your equipment and articles on emerging technologies.
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- An automatic syringe inspection machine from Seidenader combines high-voltage leak detection and vision inspection.
- A Hologram Inspection System from Advanced Vision Technology is fully automatic and combines traditional print inspection technologies, holographic foils inspection, and hologram print applications.
- The Sartocheck 4 plus Bag tester allows reliable pre-use testing of single-use bioreactors after installation based on the proven pressure-decay measurement method.
- Vetter’s filling service for sterile water-for-injection syringes is supported with five years of stability data.
- Cerno Bioscience’s MassWorks software with patented calibration technology is integrated with the DART GSX system from IonSense to provide accurate mass assignments on a mass spectrometer.
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- Aug. 13–14: MES 2013, CBI’s 8th Annual Forum on Manufacturing Execution Systems (MES) (Philadelphia, PA), unites MES professionals to discuss how to develop, deploy, and maintain an effective automation and manufacturing execution system within a regulated environment.
- Aug. 19–21: IVT’s Cleaning Validation and Critical Cleaning Processes conference (Philadelphia, PA) will discuss crucial issues, including risk assessments of multi-use equipment, understanding FDA and EMA regulations, and establishing acceptable daily exposure (ADE) limits.
- Aug. 27–28: Biotechnology 2013 (Durham, NC) by ISPE will discuss how engineers will develop and validate projects using next-generation manufacturing systems, advances in bioprocessing, and streamlined compliance programs.
- Sept. 16–18: The 2013 PDA/FDA Joint Regulatory Conference (Washington DC) will include updates from FDA speakers and case studies from pharmaceutical companies.
- Oct. 7–8: The 2013 PDA Visual Inspection Forum (Bethesda, MD) will provide interactive case studies, explore a new USP draft chapter in development for visual inspection, and discuss new developments in the field of visual inspection.
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| PharmTech Poll: Threats to Production |
What is the single greatest threat to maintaining manufacturing processes at your facility? |
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