朝阳国展北京办理医疗器械三类经营许可证没有库房怎么办包下证快捷

交申请资料到相关部门；
（2）相关部门受理申请人的申请；
（3）到实际场地进行勘察以及对产品进行审核；
（4）准予颁发三类医疗器械许可证。
2、法律依据：《医疗器械监督管理条例》第十四条
第一类医疗器械产品备案和申请第二类、第三类医疗器械产品注册，应当提交下列资料：
（一）产品风险分析资料；
（二）产品技术要求；
（三）产品检验报告；
（四）临床评价资料；
（五）产品说明书以及标签样稿；
（六）与产品研制、生产有关的质量管理体系文件；

3、法定代表人的身份证明、学历职称证明、任命文件应有效；

4、工商行政管理部门出具的《企业名称预先核准通知书》或《工商营业执照》的复印件应与原件相同，复印件确认留存，原件退回；

5、房产证明、房屋租赁证明（出租方要提供产权证明）应有效；

6、企业负责人、质量管理人的简历、学历证

it the application materials to the relevant departments; (2)the relevant departments accept the application; (3) investigatethe actual site and review the products; (4) grant the issuance ofthe third-class medical device license.2. Legal basis: Article 14of the Regulations on supervision and Administration of MedicalDevices for filing of Class I medical devices and application forregistration of Class II and Class III medical devices, thefollowing materials shall be submitted: (1) product risk analysisdata; (2) product technical requirements; (3) product technicalrequirements; (3) product inspection report; (4) clinicalevaluation data; (5) product description and label samples; (6)quality management system documents related to product developmentand production; 3. The identity certificate, academic titlecertificate and appointment documents of the legal representativeshall be valid; 4. The copy of the "Notice of Pre-approval ofEnterprise Name" or "Industrial and Commercial Business License"issued by the administrative department for industry and commerceshall be the same as the original, the copy shall be confirmed andretained, and the original shall be returned; 5. The propertycertificate and house lease certificate (the lessor shall providethe property right certificate) shall be valid; 6. Resume andquality certificate of the person in charge and quality manager