Dr Padmakar Wagh, Head- Technical Support, Waters India, gives an insight about the role of liquid chromatography
The Food & Drug administration authorities (FDA) across the globe are very particular about the quality of drug products manufactured and imported. Recently, ICH & US-FDA rolled out the quality by design (QbD) guidelines to understand the various processes and minimise the risk of potential quality related issues. Analytical method development has to align with the same guidelines to ensure that impurity profiling or chromatographic separation is risk free.
This story is from the January 16-31, 2018 edition of Express Pharma.
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This story is from the January 16-31, 2018 edition of Express Pharma.
Start your 7-day Magzter GOLD free trial to access thousands of curated premium stories, and 9,000+ magazines and newspapers.
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