Standards Promote Successful Use of Manufacturing Execution Systems
Presenters at the 8th Annual Forum on Manufacturing Execution Systems (MES) discuss how a vision and common terminology help companies implement MES globally.
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Helium Integrity Testing of Single-Use Vessels
Helium integrity testing offers advantages over pressure-decay testing for biopharmaceutical single-use vessels.
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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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Brabender Pharma USA
Brabender® Pharma USA, Inc. introduces the innovative PTSE 12/36 EC, a 12mm Stand-Alone Table-Top Twin-Screw Extruder especially designed for Hot Melt Extrusion applications. The clamshell barrel with removable barrel liner offers quick cleaning and sterilization plus easy analysis of the extrusion process. The segmented screw elements offer numerous processing capabilities and adaptability to easily meet specific needs.  Click here for details |
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Tekleen Automatic Filters Inc
TEKLEEN® self-cleaning water filters provide the ultimate solution in the pharmaceutical industry where dirty water is a problem. The filters operate on line pressure alone. The self-cleaning process is triggered by a pressure differential and is accomplished in seconds without interrupting the main flow. The TEKLEEN® filters are all offered in stainless steel construction at carbon steel prices.
For more information please visit  www.tekleen.com |
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- Oct. 7–8: 2013 PDA’s 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.
- Oct. 9–10: At the Process Validation Conference: Practical Application of the Lifecycle Approach (New Brunswick, NJ) participants will hear from industry experts and regulators instrumental in developing FDA guidelines.
- Oct. 21–23: The PDA 8th Annual Global Conference on Pharmaceutical Microbiology (Bethesda, MD) is dedicated to advancing science and regulation for global pharmaceutical microbiology.
- Oct. 22–24: IVT’s Validation Week (San Diego, CA) covers topics including validation of process, computer, equipment, method, facility, and cleaning.
- Nov. 3–6: The ISPE 2013 Annual Meeting (Washington D.C.) brings together global industry and regulatory experts to provide the latest innovative processes, technologies, and quality management techniques.
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| PharmTech Poll: Anticounterfeiting |
What anticounterfeiting tools are having the most significant effect on thwarting counterfeit drugs? |
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