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CPR認證的模式

　　System 1+ roduct certification comprising the issuing of a certificate of constancy of performance with determination of the product-type, continuous surveillance and audit testing by a notified product certification body

　　1+類：產(chǎn)品型式測試，工廠及FPC檢驗，持續(xù)監(jiān)督，檢驗

　　System 1 roduct certification comprising the issuing of a constancy of performance with determination of the product-type and continuous surveillance by a notified product certification body

　　1類：產(chǎn)品型式測試，工廠及FPC檢驗，持續(xù)監(jiān)督

　　System 2+ Factory production control certification with continuous surveillance by a notified factory production control certification body

　　2+類：工廠及FPC檢驗，持續(xù)監(jiān)督

　　System 3 Determination of product type by a notified testing laboratory

　　3類：產(chǎn)品型式測試

　　System 4 Manufacturer's tasks only.

　　4類：制造廠產(chǎn)品型式測試

　　CPR法規(guī)與CPD指令主要差異

　　- 諸多新的定義

　　- 在設(shè)定條件下CE標志成為了強制要求

　　- 進口商和分銷商需要承擔同樣的責任

　　- ETAG 和ETA(許可)將分別被EAD和ETA (評估)替代

　　- 技術(shù)評估機構(gòu)（TABs）的責任

　　- 授權(quán)機構(gòu)的責任

　　- 公告機構(gòu)（NBs）的額外責任

　　- 公告機構(gòu)授權(quán)程序

　　- 取得CE標志的相關(guān)簡化程序