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Rumors rumble on as to who will take over medtech reg file at EU Parliament

This article was originally published in Clinica

Executive Summary

There is further speculation one of two UK MEPs, Linda McAvan or Glenis Willmott,is likely to be chosen to act as rapporteur for the medical devices regulatory text when the file is reviewed again by the European Parliament during a second reading. This reading is likely to begin in September.

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