Please use this identifier to cite or link to this item: http://10.1.7.192:80/jspui/handle/123456789/6541
Full metadata record
DC FieldValueLanguage
dc.contributor.authorJain, Shashank-
dc.date.accessioned2016-06-21T08:09:46Z-
dc.date.available2016-06-21T08:09:46Z-
dc.date.issued2016-
dc.identifier.urihttp://hdl.handle.net/123456789/6541-
dc.description.abstractSince the turn of the millennium, the issue of Genotoxic Impurities (GTIs) has perhaps been one of the most emotive issues facing the Pharmaceutical Industry. Regulations for GTIs is always a great challenge to Drug regulators in the world. The Dissertation includes Introduction of GTIs & Regulatory current scenario of the GTIs. This Dissertation also includes the types of GTIs, their Classification, History alongwith some case studies. Then also performed In silico / In vivo-In vitro methods for identification of different structural alerts/drugs with plausible predicition of some drugs from different categories by using Derek Nexus & Toxtree softwares based on In silico methods. The GTIs in recent years are one of the most famous topic of concern between all the regulators in the world & its evaluation is also one of the primary concern.en_US
dc.publisherInstitute of Pharmacy, Nirma University, A'baden_US
dc.relation.ispartofseriesPDR00394;-
dc.subjectDissertation Reporten_US
dc.subjectPharmaceutical Analysisen_US
dc.subjectRegulatory Affairs & Quality Assuranceen_US
dc.subject14MPHen_US
dc.subject14MPH808en_US
dc.subjectPDR00394en_US
dc.titleA Comprehensive Study for The Regulations of Genotoxic Impurities in Pharmaceutical Drug Substances & Products with Special Reference to Their Detection, Identification and Evaluationeen_US
dc.typeDissertationen_US
Appears in Collections:M.Pharm. Research Reports, Pharmaceutical Analysis

Files in This Item:
File Description SizeFormat 
PDR00394.pdfPDR003946.46 MBAdobe PDFThumbnail
View/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.