- 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
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【培訓(xùn)流程】:報(bào)名→交納費(fèi)用→學(xué)習(xí)考試→取得證書
【考核發(fā)證】:考試合格者頒發(fā)認(rèn)可的內(nèi)部審核員資格證書,證書電子注冊(cè),網(wǎng)上查詢真?zhèn)?,全國企業(yè)通用。
【培訓(xùn)費(fèi)用】:1000元(電子教材),1200元(電子教材+書面教材)。
【證 書】:證書學(xué)員身份號(hào),獨(dú)有編號(hào),網(wǎng)上查詢,全國通用。
【報(bào)名資料】:報(bào)名請(qǐng)交納一寸彩照2張、身份證復(fù)印件1張。
【證書樣本】:
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