Developments in Pharmaceutical Process Modeling
Model-predictive design is applied to solid-dosage processes.
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Now Online To read about methods for identifying out-of-trend results in ongoing stability data, read the online article from the June issue of Pharmaceutical Technology.
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Predicting Glass Delamination
A screening method predicts delamination in primary packaging.
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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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- The Empower 3 Chromatography Data Software from Waters now features mobile access to chromatography systems from a tablet or smartphone.
- The Accelrys Enterprise Platform 9.0 is an open, scientifically aware platform capable of managing “big data” and externalized research-collaboration networks.
- Novatek EM-Mobile combines an environmental-monitoring application from Novatek with an Xplore iX104C5 DMCR (Dual-Mode Clean Room) rugged tablet from Xplore Technologies to provide the real-time information needed to manage the pharmaceutical manufacturing process.
- The Malvern Viscotek viscometer detector enhances gel permeation/size exclusion chromatography (GPC/SEC) for analyzing polymers, including those used in pharmaceutical applications.
- The Cole-Parmer MS-3400 centrifuges include benchtop and portable models.
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- June 24–26: The 11th Product Complaints Congress for the Life Sciences (Washington, DC) discusses best practices for handling product complaints and regulatory requirements.
- June 27–28: The 8th annual Global Pharma Manufacturing Summit 2013 (Boston, MA) gathers industry leaders in small molecule and biologic pharmaceutical manufacturing to discuss best practices in streamlining production processes.
- July 10–11: PDA Europe’s Current and Emerging EU Regulations and Inspection Trends (Dublin, Ireland) will discuss upcoming regulations and their impact on the pharmaceutical industry.
- July 18: USP’s Analysis of Elemental Impurities (Minneapolis, MN) will cover the revisions of USP chapters <232> and <233> for analysis of elemental impurities in pharmaceutical materials.
- 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.
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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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