Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/12446
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dc.contributor.authorMahajan, Madhur Mohit-
dc.date.accessioned2011-07-22T06:56:10Z-
dc.date.available2011-07-22T06:56:10Z-
dc.date.issued2011-07-
dc.identifier.issn0975-1076 (Online); 0971-7544 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/12446-
dc.description321-329en_US
dc.description.abstractIndia, being a signatory of WTO agreements, has moved from no or partial patent protection to full fledged patent protection. This represents a radical break from the past in which developing countries typically had only weak levels of patent protection. In this context, this research examines the steps involved in development of R&D capabilities in the Indian pharmaceutical firms as a response to strengthening of patent law. This paper analyses the post-TRIPS behaviour of domestic pharmaceutical firms in India with respect to R&D intensification, development of new molecules and enhanced DMF filings. The study establishes that firms in the post WTO era have increased their R&D efforts tremendously and are moving towards the development of advance level process and product R&D capabilities. Such firms have also opted for vigorous DMF filings abroad reflecting qualitative modifications and adjustments in its R&D capabilities in the production of exportables.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceJIPR Vol.16(4) [July 2011]en_US
dc.subjectTRIPSen_US
dc.subjectInnovationen_US
dc.subjectNCEen_US
dc.subjectDMFen_US
dc.titleThe Emergence of New R&D Paradigms in the Indian Pharmaceutical Industry: Post TRIPS Perioden_US
dc.typeArticleen_US
Appears in Collections:JIPR Vol.16(4) [July 2011]

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