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Analytical Process Isolator

Virus Screening & HPAPI Handling-The Analytical Process Isolator

Analytical Process Isolator™ Continuous Process Isolator for Virus Screening & HPAPI Handling Contact Our Experts Process Allows for ISO 5 processing and intake/outtake through a negative pressure cabinet. Containment Surrogate powder test results show containment below 10 ng/m3, even with large spills.  Design The chamber on the right is a vented balance enclosure (VBE) for …

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Less Downtime, More Productivity: FSI Systems Cost of Ownership

Flow Sciences, a leading provider of containment systems for laboratory, pilot plant, and manufacturing facilities, delivers low cost of ownership and high return on investment. By utilizing sophisticated engineering and design into the construction of the systems, they are able to achieve less lab downtime, more consistent results, no cross-contamination, and less energy consumption. Q: …

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Stainless Steel Malvern 3000 Enclosure

Application: Small Volume Liquid Dispersion Analysis with Getinge La Calhene Alpha-Beta Ports This stainless steel enclosure was designed for small volume liquid dispersion/particle size distribution analysis methods involving Highly Potent Active Pharmaceutical Ingredients (HPAPIs). Particularly, it was designed for operations conducted in facilities operating under the stipulations of current Good Manufacturing Practices (cGMPs). The working …

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Thinking Outside the Box: 10 Considerations For Balance Stability

ABSTRACT: Stability of your weighing balance is paramount when it comes to collecting reliable data for project. As the old adage goes, “Anything that can go wrong will go wrong.”. Depending on the problem, taking obvious action for a seemingly obvious solution may not result in success. The purpose of this paper is to inspire …

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Red Lights and Green Lights – The Keys to Superior Containment in Compounding Applications

Abstract: In a previous White Paper 2, we reviewed in detail how Flow Sciences vented balance enclosures can allow accurate measurement of samples in the range of 0.1 mg to 0.1 µg. In this paper, we will review why very bad things happen when either quantity or purity of Highly Potent Active Pharmaceuticals is not properly maintained …

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