What Type of European Representative (EU REP) Should Be for Medical Devices and Non Medical Devices?

 میڈیکل ڈِوِائِس اور Non میڈیکل ڈِوِائِس کے لیے EU REP کس قسم کا ہونا چاہیے؟


GPSR کے اندر نارمل پروڈکٹس کون سی ہیں اور High Risk کون سی ہیں؟

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