&

啊啊啊啊好爽欧美_亚洲av春色av_a特级片久久艹久久艹_国产普通话对白在线香蕉

Registration Service of Medical Devices: CRC services Medical Device Business License Medical Device Registration Contract Research Organization ISO 13485 Quality System Certification GMP CE Certification Service FDA Registration (Filing) Software Integrity Verification Service Production process validation service ISO 15378 Medical Package System Certification ISO 13485 Internal Auditors Training Regulatory Services For Medical Devices
Information security service of medical: ISO 27001 Information Security Certification ISO 20000 Information Service Certification Information system grade protection filing Business Continuity Management Services Internal Auditor Training
Medical Software Development: Software of Good Supply Practice(GSP) Production System Development Customized software development

CONTACT US

Current location: Default>Services>Medical Device Registration

醫(yī)療器械注冊變更

CREATE TIME:2018-07-04 15:49BROWSE TIMES:3561

根據(jù)《醫(yī)療器械監(jiān)督管理?xiàng)l例》（國務(wù)院令第650號(hào)）的規(guī)定，已注冊的第二類、第三類醫(yī)療器械，醫(yī)療器械注冊證及其附件載明的內(nèi)容發(fā)生變化，申請人應(yīng)當(dāng)向原注冊部門申請注冊變更，并按照相關(guān)要求提交申報(bào)資料。

標(biāo)簽：醫(yī)療器械注冊、一類醫(yī)療器械注冊、二類醫(yī)療器械注冊咨詢、三類醫(yī)療器械產(chǎn)品注冊

PREVIOUS: NOTHING
NEXT: 醫(yī)療器械首次注冊流程