三、現場(chǎng)提交成功后約去現場(chǎng)勘察，現場(chǎng)需提交材料

1）崗位職責

2）工作程序

3）公司制度

4）供應商檔案

5）培訓記錄

6）新法律法規

7）員工檔案等

現場(chǎng)核查成功后一周內就可以拿證了。

我公司主要經(jīng)營(yíng)代辦北京醫療器械公司注冊|代辦北京三類(lèi)醫療器械公司注冊|代辦北京二類(lèi)醫療器械備案憑證|代辦北京食品經(jīng)營(yíng)許可證|代辦北京醫療器械網(wǎng)絡(luò )備案|代辦北京輻射安全許可等資質(zhì)專(zhuān)項審批服務(wù)

三類(lèi)醫療器械指的是植入人體，用于支持、維持生命，對人體具有潛在危險，對其安全性、有效性必須嚴格控制的醫療器械?，F行制度規范下，經(jīng)營(yíng)三類(lèi)醫療器械的經(jīng)營(yíng)主體需要按程序辦理三類(lèi)醫療器械經(jīng)營(yíng)許可證。

yee files, etc You can get the certificate within a week after the successful on-site verification. My company main business agent Beijing medical e company registration | agent Beijing three types of medical device company registration | agent Beijing class medical e for the record certificate | Beijing food business license | Beijing medical e network for the record | Beijing radiation safety license special examination and approval services Class III medical devices refer to the medical devices implanted in human body to support and maintain life, with potential danger to human body, and their safety and effectiveness must be strictly controlled. Under the current system and norms, the business entities of th