MDR European Authorised Representative Template
The European Commission in the Medical Device Regulations (MDR) has imposed many legal obligations on you the European Medical Device Authorised Representatives. These legal obligations require you the Authorised Representative to maintain several registers which include, but are not limited to, Complaints, Device Verification, Class III implantable, and Vigilance.
Following direct industry requests Eudamed.eu using their extensive MDR and EUDAMED experience have prepared spreadsheet templates specifically for you the Authorised Representative. These templates will assist you in meeting your many legal obligations.
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