Latest Whitepapers

Why automated image analysis is rapidly replacing manual microscopy for characterizing particle shape and how combining it with Raman spectroscopy adds chemical identification.

In this white paper, our marketing director of the America’s Kathy Macchiarola outlines the important decisions factors that are key requirements and help you select a benchtop system ideal for your situation and your needs.

The purpose of this document is to describe how PANalytical systems support system owners meeting the requirements of the 21 CFR Part 11 regulations issued by the United States’ FDA.

The recent changes to the United States Pharmacopeia (USP) regarding requirements for elemental impurity testing has peaked interest into new ways to perform this testing. Combining these new requirements with the introduction of USP chapter <735> X-ray fluorescence spectrometry1 permits a new alternate method for quantifying elemental impurities in pharmaceutical materials.

Download this free white paper from Protein Simple to learn about the differences between MFI and how MFI provides crucial information about your protein therapeutic.

The accuracy and completeness of data is crucial for safe product development and to prevent serious implications regarding human health.

Data analysis process aiming at the identification of lipid biomarkers and the
evaluations of their performance.

Understanding the key methods to help prevent particle sizing failures using laser diffraction.

Applying standard microscopy techniques on 3D cell cultures can be challenging. This white paper demonstrates how RAFT™ 3D Cell Cultures can be visualized with subcellular resolution under a standard fluorescence microscope.

Here are some questions you should ask yourself as you begin evaluating
dynamic light scattering instruments.