- 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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工藝驗(yàn)證:從工藝設(shè)計(jì)階段到商業(yè)生產(chǎn)的整個(gè)過程中,對(duì)數(shù)據(jù)進(jìn)行收集和評(píng)價(jià),建立工藝能始終如一地交付出優(yōu)質(zhì)產(chǎn)品中的科學(xué)證據(jù)。工藝驗(yàn)證涉及整個(gè)產(chǎn)品生命周期和生產(chǎn)中發(fā)生的一系列活動(dòng)。包括3階段:
第一階段 - 工藝設(shè)計(jì):在開發(fā)和放大活動(dòng)過程中獲得的知識(shí)基礎(chǔ)上,在此階段對(duì)商業(yè)化生產(chǎn)工藝進(jìn)行定義。
第二階段 - 工藝確認(rèn):在此階段,對(duì)工藝設(shè)計(jì)進(jìn)行評(píng)估,以確認(rèn)工藝是否具備可重現(xiàn)的商品化制造能力。
第三階段 - 持續(xù)工藝確認(rèn):在日常生產(chǎn)中獲得工藝處于受控狀態(tài)的持續(xù)的保證。
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