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Article 42-2Reproduction for Examination and Similar Proceedings; Related Matters

第四十二条の二(審査等の手続における複製等)

It is permissible to reproduce a work if and to the extent that this is found to be necessary for the following proceedings; provided, however, that this does not apply if the action would unreasonably prejudice the interests of the copyright owner in light of the nature and purpose of the work, the number of copies that would be made, and the circumstances of its reproduction:

著作物は、次に掲げる手続のために必要と認められる場合には、その必要と認められる限度において、複製することができる。ただし、当該著作物の種類及び用途並びにその複製の部数及び態様に照らし著作権者の利益を不当に害することとなる場合は、この限りでない。

proceedings involved in a patent, industrial design, or trademark examination, the technical valuation of a utility model, or an international search or international preliminary examination for an international application (meaning international applications provided for in ) by an administrative agency;

行政庁の行う特許、意匠若しくは商標に関する審査、実用新案に関する技術的な評価又は国際出願(に規定する国際出願をいう。)に関する国際調査若しくは国際予備審査に関する手続

proceedings regarding an administrative agency's examination of a variety (meaning the variety as provided in ) or investigation of a registered variety (meaning the registered variety as provided in );

行政庁の行う品種(に規定する品種をいう。)に関する審査又は登録品種(に規定する登録品種をいう。)に関する調査に関する手続

proceedings regarding an administrative agency's registration of specific agricultural, forestry and fishery products and foodstuffs (meaning specific agricultural, forestry and fishery products and foodstuffs as provided in ; hereinafter the same applies in this item) under or designation of specific agricultural, forestry and fishery products and foodstuffs of foreign countries under ;

行政庁の行う特定農林水産物等(に規定する特定農林水産物等をいう。以下この号において同じ。)についてのの登録又は外国の特定農林水産物等についてのの指定に関する手続

proceedings regarding an administrative agency's or incorporated administrative agency's examination or investigation of pharmaceutical affairs (the pharmaceutical affairs include particulars of medical devices (meaning medical devices as provided in ) and regenerative medicine products (meaning regenerative medicine products as provided in ); the same applies hereinafter in this item), or proceedings regarding a report about pharmaceutical affairs submitted to an administrative agency or incorporated administrative agency;

行政庁若しくは独立行政法人の行う薬事(医療機器(に規定する医療機器をいう。)及び再生医療等製品(に規定する再生医療等製品をいう。)に関する事項を含む。以下この号において同じ。)に関する審査若しくは調査又は行政庁若しくは独立行政法人に対する薬事に関する報告に関する手続

beyond what is set forth in the preceding items, proceedings that Cabinet Order prescribes as being similar thereto.

前各号に掲げるもののほか、これらに類するものとして政令で定める手続

It is permissible to make a public transmission of a work or to publicly communicate it through a receiver, to the extent that this is found to be necessary for the proceedings set forth in the items of the preceding paragraph that are conducted using electronic or magnetic records or accompanied by the transmission and reception of images or sounds; provided, however, that this does not apply if the action would unreasonably prejudice the interests of the copyright owner in light of the nature and purpose of the work and the circumstances of its public transmission or communication.

著作物は、電磁的記録を用いて行い、又は映像若しくは音声の送受信を伴つて行う前項各号に掲げる手続のために必要と認められる場合には、その必要と認められる限度において、公衆送信を行い、又は受信装置を用いて公に伝達することができる。ただし、当該著作物の種類及び用途並びにその公衆送信又は伝達の態様に照らし著作権者の利益を不当に害することとなる場合は、この限りでない。

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