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EU One Step Closer To Confirming EMA's New Pivotal Role In Device Matters

 
• By Amanda Maxwell

Industry opposes the proposed new role of European Medicines Agency in overseeing devices availability in a healthcare crisis. But a new Regulation may be adopted in March and its fallout looks set to herald a new era for device supply management and regulation.

EMA

In light of the health care product supply challenges during the current pandemic, the European Parliament and the Council of the EU have reached a provisional agreement on the European Commission’s proposed Regulation for a reinforced role for the European Medicines Agency in healthcare crises.

The document lays out the new role the EMA would play in overseeing various aspects of device management, as well...

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