Advanced analytical methods are speeding up the targeted evaluation of potential viral contaminants.

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The Challenge of Finding the Unknown

Methods must be suitable at each development phase, robust, and effective on multiple platforms.

Keys to Successful Method Transfer

Analytical procedures and method validation should be developed with a structured and rigorous approach.

AQbD Adds Rigor to Method Development

The authors present a validation study of an analytical method for the simultaneous determination of nine human cytokines in human K2-EDTA plasma.

Validation of a Multiplex Bead-Based Assay

 (USP) <232> will require measurement of elemental impurities using inductively coupled plasma–mass spectrometry (ICP–MS). The authors describe a rapid, single-point calibration approach for ICP–MS analysis of raw materials used in drug product manufacturing.

The authors describe a rapid, single-point calibration approach for ICP–MS analysis of raw materials used in drug product manufacturing.

Rapid Screening for Elemental Impurities using ICP-MS

Industry players form Allotrope Foundation to solve analytical data management problems.

Standardizing Data Management

Recent technology introductions demonstrate that accuracy, efficiency, and usability are top of mind for pharmaceutical industry professionals for analytical instruments.
	 

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