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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
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醫療器械注冊變更

CREATE TIME:2018-07-04 15:49BROWSE TIMES:3563

根據《醫療器械監督管理條例》（國務院令第650號）的規定，已注冊的第二類、第三類醫療器械，醫療器械注冊證及其附件載明的內容發生變化，申請人應當向原注冊部門申請注冊變更，并按照相關要求提交申報資料。