Industry Pipeline - Pharmaceutical Technology

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PharmTech Europe

Industry Pipeline
Interphex Showcase 2010.

Pharmaceutical Technology
Volume 34, Issue 4, pp. 128-135

MANUFACTURING EQUIPMENT & SUPPLIES



Sanitary ball valve
Lee Industries's T-316 stainless-steel highly sanitary-ball valve meets the qualifications of the pharmaceutical industry. Rigid corrosion-resistant and solid construction provides reliability under extreme conditions. A simple fast-breakdown design helps reduce cleanup and maintenance costs. Lee Industries, Philipsburg, PA http://www.leeind.com/ tel. 814.342.0461



Fluid-path assemblies
One-Touch single-use fluid-path assemblies are designed for secure fluid transfer in critical biopharmaceutical processing applications. The products can be customized to end-user requirements and include combinations of connectivity, tubing, and other components. Fluid paths can be integrated with filter capsules in various surface areas, end-connection configurations, and media. Meissner Filtration Products, Camarillo, CA http://www.meissner.com/ tel. 805.388.9911



Culturing set
SGM's DriAmp biological-indicator culturing set features Releasat medium and is designed for high-temperature, direct-air exposure or submersion in nonwater-based solutions. The DriAmp BI is a 1-mL, snap-top glass ampul containing inoculated silica. The Releasat medium provides a reduced incubation time of 72 h. A color change indicates positive test results. SGM Biotech, Inc., Bozeman, MT http://www.sgmbiotech.com/ tel. 406.585.9535



Visual inspection system
Eisai Machinery USA offers semiautomatic, semimanual, and manual VIS visual inspection systems. Eisai provides validation expertise to help implement VIS 1000 semiautomatic inspection machines. The company also provides a program of continuous service and technical support for its clients. The program monitors clients' machines to reduce downtime and improve production-line efficiency. Eisai Machinery USA, Hackensack, NJ http://www.eisaiusa.com/ tel.201.746.2111


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Survey
FDASIA was signed into law two years ago. Where has the most progress been made in implementation?
Reducing drug shortages
Breakthrough designations
Protecting the supply chain
Expedited reviews of drug submissions
More stakeholder involvement
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View Results
Eric Langerr Outsourcing Outlook Eric LangerRelationship-building at Top of Mind for Clients
Cynthia Challener, PhD Ingredients Insider Cynthia ChallenerRisk Reduction Top Driver for Biopharmaceutical Raw Material Development
Jill Wechsler Regulatory Watch Jill Wechsler Changes and Challenges for Generic Drugs
Faiz Kermaini Industry Insider Faiz KermainiNo Signs of a Slowdown in Mergers
From Generics to Supergenerics
CMOs and the Track-and-Trace Race: Are You Engaged Yet?
Ebola Outbreak Raises Ethical Issues
Better Comms Means a Fitter Future for Pharma, Part 2: Realizing the Benefits of Unified Communications
Better Comms Means a Fitter Future for Pharma, Part 1: Challenges and Changes
Source: Pharmaceutical Technology,
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