Critical factors in manufacturing multi-layer tablets-Assessing material attributes, in-process controls, manufacturing process and product performance
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作者:
Vaithiyalingam, Sivakumar R.
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US FDA, Div Chem 3, OGD, Ctr Drug Evaluat & Res, Rockville, MD USAUS FDA, Div Chem 3, OGD, Ctr Drug Evaluat & Res, Rockville, MD USA
Vaithiyalingam, Sivakumar R.
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Sayeed, Vilayat A.
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US FDA, Div Chem 3, OGD, Ctr Drug Evaluat & Res, Rockville, MD USAUS FDA, Div Chem 3, OGD, Ctr Drug Evaluat & Res, Rockville, MD USA
Sayeed, Vilayat A.
[1
]
机构:
[1] US FDA, Div Chem 3, OGD, Ctr Drug Evaluat & Res, Rockville, MD USA
Advancement in the fields of material science, analytical methodologies, instrumentation, automation, continuous monitoring, feed forward/feed back control and comprehensive data collection have led to continual improvement of pharmaceutical tablet manufacturing technology, notably the multi-layer tablets. This review highlights the material attributes, formulation design, process parameters that impact the performance, and manufacturability of the multi-layer tablets. It also highlights on critical-to-quality elements that needs to be addressed in the regulatory submission. Published by Elsevier B.V.