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Sample Preparation
Last updated: November 2023
Quality control (QC) is a critical step in the biopharmaceutical industry.
Each manufacturer must demonstrate that its drugs are consistently produced, safe, potent, and pure. The number of tests that must be run by QC labs continues to rise to meet the ever-increasing QC requirements of global regulatory agencies.
Download this infographic to learn four ways to immediately improve the quality of your samples for common QC assays, including high pressure liquid chromatography (HPLC), liquid chromatography– mass spectrometry, ion chromatography (LC-MS, IC), or inductively coupled plasma mass spectrometry (ICP-MS).
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Sample preparation technique refers to the way samples are treated to be readied for analysis. These methods include sample extraction, pre-concentration and crushing and dissolution.
Quality control samples are taken from production batches into the testing process to ensure the batch is according to specifications. The purpose of QC is confirm that the new batch meets the quality level of each production batch.
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