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Medical Devices Medical Device Coordination Group Documented 202221MDCG 202221 GUIDANCE ON PERIODIC SAFETY UPDATE REPORT (POUR) ACCORDING TO REGULATION (EU) 2017/745 (MDR) December 2022This document
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Regulatory affairs professionals
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What is new mdcg guidance on?
The new MDCG guidance is on the implementation of medical device regulations.
Who is required to file new mdcg guidance on?
Manufacturers, authorized representatives, and other stakeholders involved in the medical device industry are required to file new MDCG guidance.
How to fill out new mdcg guidance on?
The new MDCG guidance can be filled out online through the designated platform provided by the regulatory authorities.
What is the purpose of new mdcg guidance on?
The purpose of the new MDCG guidance is to provide clarity and guidance on the implementation of new medical device regulations.
What information must be reported on new mdcg guidance on?
The new MDCG guidance requires reporting of details related to device classification, compliance with regulations, and other relevant information.
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