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

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

Integrity tests with a high sensitivity (Container Closure Integrity Testing, CCIT) for the pharmaceutical industry

The quality and effectiveness of drugs significantly depends on their proper packaging: more

Bioburden and Biofilm Management in Pharmaceutical Operations

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

Ultrapure Water for HPLC Analysis

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

Preparation of Standards – with the Cubis® MSA Dosing System

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

All white papers

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

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

Bioburden and Biofilm Management in Pharmaceutical Operations

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

Ultrapure Water for HPLC Analysis

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

Preparation of Standards – with the Cubis® MSA Dosing System

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

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

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

All white papers on laboratory

Integrity tests with a high sensitivity (Container Closure Integrity Testing, CCIT) for the pharmaceutical industry

The quality and effectiveness of drugs significantly depends on their proper packaging: more

Bioburden and Biofilm Management in Pharmaceutical Operations

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

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

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

Streamlining Affinity Analysis for Accelerated Biologics Development and Production

ForteBio offers the true microfluidic-free alternative to SPR for high-throughput, label-free quantitation and kinetic characterization of biologics more

Advance Lot Release and In-process Testing of Biologics in QC

ForteBio offers 21 CFR Part 11 software and full GxP products and services for Octet® instruments. Discover the benefits of label-free analytics. more

All white papers on process
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