Please use this identifier to cite or link to this item: https://ah.lib.nccu.edu.tw/handle/140.119/117183
DC FieldValueLanguage
dc.contributor科管智財所zh_TW
dc.creator陳秉訓zh_TW
dc.creatorChen, Ping-Hsunen_US
dc.date2017-07
dc.date.accessioned2018-05-17T08:47:50Z-
dc.date.available2018-05-17T08:47:50Z-
dc.date.issued2018-05-17T08:47:50Z-
dc.identifier.urihttp://nccur.lib.nccu.edu.tw/handle/140.119/117183-
dc.description.abstractThe Trans-Pacific Partnership (“TPP”) Agreement mandates member states to implement a patent linkage system vested in Article 18.53. To successfully join the TPP Agreement, Taiwan has begun the legislation of a patent linkage system by proposing an amendment for the Pharmaceutical Affairs Act. Article 18.53 requires a member either to adopt a notification mechanism under Paragraph 1 or to stay the issuance of marketing approval under Paragraph 2. But, Taiwan’s proposal includes both measures. Taiwan’ patent linkage system allows a pioneer drug company to register patents claiming (a) a material; (b) a combination or formula; or (c) pharmaceutical use. The scope of patentees who may benefit from the mechanism is larger than what is required. In addition, the system requires a generic drug company to notify the patentee at the time of filing the drug application if the generic drug company asserts invalidity or non-infringement which the generic drug company must prove. Furthermore, the health authority is allowed to stay the issuance of a generic drug permit while the patentee is suing the generic drug company in the court.en_US
dc.format.extent648776 bytes-
dc.format.mimetypeapplication/pdf-
dc.relationJournal of Law and Health, Vol.30, No.1, pp.55-79zh_TW
dc.titleAnalysis of the Proposed TPP-Related Patent Linkage System in Taiwanen_US
dc.typearticle
item.fulltextWith Fulltext-
item.openairetypearticle-
item.grantfulltextrestricted-
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
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