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Finland’s medical device functions transfer set for November

This article was originally published in RAJ Devices

Executive Summary

The transfer of Finland’s medical device regulatory functions from the National Agency for Medicines to a new welfare and health supervisory authority will take place on 1 November1.

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October and November 2020 were bad months for companies seeking to have their planned EU filings fast-tracked through the centralized drug review system at the European Medicines Agency.

EU Accelerated Assessment Tracker

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A number of companies have sought to convince the European Medicine Agency that their drug merits a fast-track regulatory review.

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