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  5. 2024-2025
Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1667
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dc.contributor.authorAKTU-
dc.date.accessioned2025-10-17T09:33:11Z-
dc.date.available2025-10-17T09:33:11Z-
dc.date.issued2025-10-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1667-
dc.descriptionBP702T B.Pharma (SEM VII)en_US
dc.language.isoen_USen_US
dc.publisherAKTUen_US
dc.subjectBP702T INDUSTRIAL PHARMACY II THEORYen_US
dc.subjectincluding Scale-Up, Technology Transfer, Packaging Technology, Quality Assurance, Quality Risk Management, Process Validation, GMP, Regulatory Affairs, New Drug Applications (NDAs), Good Laboratory Practices (GLP), and specific Indian regulations like those from the CDSCOen_US
dc.titleBP702T INDUSTRIAL PHARMACY II THEORYen_US
dc.title.alternativeBP702T B.Pharma (SEM VII)en_US
dc.typeOtheren_US
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