Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/9695
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dc.contributor.authorSoni, Rutwa Yogesh-
dc.date.accessioned2021-02-01T08:14:58Z-
dc.date.available2021-02-01T08:14:58Z-
dc.date.issued2020-05-
dc.identifier.urihttp://10.1.7.192:80/jspui/handle/123456789/9695-
dc.publisherInstitute of Pharmacy, Nirma University, A'baden_US
dc.relation.ispartofseriesPDR00615;-
dc.subjectDissertation Reporten_US
dc.subjectPharmaceutical Analysisen_US
dc.subjectRegulatory Affairsen_US
dc.subject18MPHen_US
dc.subject18MPH805en_US
dc.subjectPDR00615en_US
dc.titleRegulatory Requirements For Drug Product Registration and Life Cycle Management For Parenterals: INDIA, USA and EUROPEen_US
dc.typeDissertationen_US
Appears in Collections:M.Pharm. Research Reports, Pharmaceutical Analysis

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