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DC Field | Value | Language |
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dc.contributor.author | Jain, Shashank | - |
dc.date.accessioned | 2016-06-21T08:09:46Z | - |
dc.date.available | 2016-06-21T08:09:46Z | - |
dc.date.issued | 2016 | - |
dc.identifier.uri | http://hdl.handle.net/123456789/6541 | - |
dc.description.abstract | Since 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.publisher | Institute of Pharmacy, Nirma University, A'bad | en_US |
dc.relation.ispartofseries | PDR00394; | - |
dc.subject | Dissertation Report | en_US |
dc.subject | Pharmaceutical Analysis | en_US |
dc.subject | Regulatory Affairs & Quality Assurance | en_US |
dc.subject | 14MPH | en_US |
dc.subject | 14MPH808 | en_US |
dc.subject | PDR00394 | en_US |
dc.title | A Comprehensive Study for The Regulations of Genotoxic Impurities in Pharmaceutical Drug Substances & Products with Special Reference to Their Detection, Identification and Evaluatione | en_US |
dc.type | Dissertation | en_US |
Appears in Collections: | M.Pharm. Research Reports, Pharmaceutical Analysis |
Files in This Item:
File | Description | Size | Format | |
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PDR00394.pdf | PDR00394 | 6.46 MB | Adobe PDF | ![]() View/Open |
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