中英文對(duì)照—醫(yī)療器械經(jīng)營(yíng)企業(yè)設(shè)立流程-wenkub
2023-06-10 01:22:04 本頁(yè)面
【正文】 ） ?Administrative License Application 行政許可事項(xiàng)申請(qǐng)書(shū) ?Feasibility Study Report 可行性研究報(bào)告 ?Letter of Authorization for Receiving Legal Documents法律文件送達(dá)授權(quán)委托書(shū) ?Notification of Preapproval of Enterprise Name企業(yè)名稱(chēng)預(yù)先核準(zhǔn)通知書(shū) ?List of the legal representative or board of directors外資企業(yè)法定代表人（或董事會(huì)人選）名單 ? Letter of Authorization and the Copy of ID Card of mandatary授權(quán)委托書(shū)及受托人身份證復(fù)印件 ? Articles of Association,Identity certificates of foreign investors or legal qualification certificate of the corporation and Certificate of Credit Status 外資企業(yè)章程，經(jīng)公證和依法認(rèn)證的境外投資者身份證明文件或注冊(cè)登記證明及資信證明文件 ?Approval by Development and Reform Commission發(fā)展改革部門(mén)做出的項(xiàng)目核準(zhǔn)批復(fù) STEP3 Medical equipment business License （醫(yī)療器械經(jīng)營(yíng)許可證） Time Scale: About 30 working days Department Required documents ?Application for Medical equipment business License 醫(yī)療器械經(jīng)營(yíng)許可證申請(qǐng)表 ?Certificate for Preapproval Registration of Enterprise Name企業(yè)名稱(chēng)預(yù)先核準(zhǔn)通知書(shū) ?Organization and Function 組織機(jī)構(gòu)與職能 ?File directory of Product quality management regulation 產(chǎn)品質(zhì)量管理制度文件目錄 ?Letter Authorization signed by Enterprise 企業(yè)簽署的授權(quán)委托書(shū) ?Statement of Guarantee on the Authenticity of the Information Submitted 材料真實(shí)性保證聲明 ?ID card, Diploma or Professional title certificate of quality managers (Original and copy) and their resume 質(zhì)量管理人員的身份證、學(xué)歷或者職稱(chēng)證明原件和復(fù)印件及個(gè)人簡(jiǎn)歷 ?Registered address and the location map and plans (specify area) of warehouse and the copy of Real estate ownership certification or other Certificate of rights t
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