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.
この記事は Express Pharma の January 16-31, 2018 版に掲載されています。
7 日間の Magzter GOLD 無料トライアルを開始して、何千もの厳選されたプレミアム ストーリー、9,000 以上の雑誌や新聞にアクセスしてください。
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この記事は Express Pharma の January 16-31, 2018 版に掲載されています。
7 日間の Magzter GOLD 無料トライアルを開始して、何千もの厳選されたプレミアム ストーリー、9,000 以上の雑誌や新聞にアクセスしてください。
すでに購読者です? サインイン
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