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欧盟医疗器械指令_MDD_93-42-EEC(中英文)

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6. 各会员国或执委会如认为协调标准不完全符合第三条所述的基本要求时, 会员国针对这些标准所采取的措施及本条第一项的公布事宜应依第六条第二项的程序进行.Article 6 第 6 条Committee on Standards and Technical Regulations 标准及技术法规委员会1. mission shall be assisted by mittee set up by Article 5 of Directive 83/189/EEC. 依据83/189/EEC号指令第五条所设立的委员会应给予执委会协助. 2. The representative of mission shall submit to mittee a draft of the measures to be taken. mittee shall deliver its opinion on the draft within a time limit which the chairman may lay down according to the urgency of the matter, if necessary by taking a vote. 执委会代表应将欲采取行的方法的草案提交委员会, 委员会应于特定期限内提出其意见, 期限的长短可由委员会主席依事情紧急的程度决定, 必要时得采取表决方式决定.The opinion shall be recorded in the minutes; in addition, each Member State shall have the right to ask to have its position recorded in the minutes. 委员会的意见应详细记录: 除此的外, 各会员国代表得要求详细记录其持立场.

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