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Weighing in Pharmaceutical Quality Control according to U.S. Pharmacopeia

USP Chapter 41 Weighing Requirements on Balances in Pharmceutical Quality Control

19-Jun-2019

USP Chapter 41 weighing requirements are mandatory in a Pharmaceutical Quality Control laboratory, where weighing is a fundamental step.

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Bioburden and Biofilm Management in Pharmaceutical Operations

Perspective of Aseptic Sampling

14-May-2019

Microbial control is a major objective for all sterile drug manufacturers, with bioburden reduction representing a significant share of risk mitigation efforts

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Preparation of Standards – with the Cubis® MSA Dosing System

100% traceability in compliance with GLP and accredited procedures

14-May-2019

Reference samples, called standards, are required to determine the concentration of chemical compounds using highly sensitive quantitative analytical procedures

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Ultrapure Water for HPLC Analysis

No ghost peaks – for optimal results

14-May-2019

Learn how to optimize your application and minimize the risk of ghost or phantom peaks.

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You’re using surfactants like Triton X-100? The REACH clock is ticking …

Download information to see your options, including suggested alternatives to NPEs and OPEs

02-May-2019

It’s time to act if you are using alkylphenol ethoxylate (APE) surfactants such as nonylphenol ethoxylates (NPEs) and octylphenol ethoxylates (OPEs)

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How to Save 80% Costs of Continuous Small Molecule and Biomolecule Purification

Simulated moving bed chromatography (SMBC) for higher productivity and significantly lower costs

30-Apr-2019

Simulated moving bed chromatography (SMBC) is an HPLC technique that continuously separates substance mixtures and extracts them into two fractions

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Minimum Space Requirement – Maximum Detection Efficiency

POC diagnosis: Compact multispectral sensor delivers fast, medically specific test results

04-Mar-2019

Learn how the multispectral PixelSensor™ is revolutionizing sophisticated point-of-care testing in healthcare

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ETC Powder Dispensing Study

Automated powder dispensing to increase R&D efficiency

25-Feb-2019

Can an automated powder dosing solution in the pharmaceutical industry meet the re-quirements of applications, and which system is best suited?

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The Diffusion Interaction Parameter (kD) as an Indicator of Colloidal and Thermal Stability

19-Feb-2019

The experiment shown here illustrates how thermal and colloidal stability can be measured simultaneously

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Robust and Repeatable Nanoparticle Drug Delivery Characterization with FFF-MALS-DLS

19-Feb-2019

This article highlights a study demonstrating the benefits of FFF-MALS-DLS for the char- acterization of nanolipid particles

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