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MHRA UKRP Requirements For US Med Device Companies To Enter The UK Market

MHRA UKRP Requirements For US Med Device Companies To Enter The UK Market
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EU MDR And IVDR Implementation: New Transitional Regime Enters Into Force | MoFo Life Sciences

On March 20, 2023, the new transitional regime for medical devices in the EU and the EEA became effective when Regulation (EU) 2023/607 (the “Regulation”) was published in the Official.

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EU regulatory changes impacting the life sciences industry in 2023

Head of EU regulatory life sciences team at law firm Cooley looks at five major EU regulatory milestones for the life science sector in 2023.

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EU MDR And IVDR Implementation: European Commission Publishes Full Proposal For Amending Transitional Regime | MoFo Life Sciences

Following up on its announcement in the EU Employment, Social Policy, Health and Consumer Affairs Council (EPSCO) Meeting, the European Commission (Commission) released on January 6,.

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European Commission Proposes Amending Transitional Provisions in Medical Devices and In Vitro Diagnostics Regulations | Cooley LLP

On 6 January 2023, the European Commission adopted a proposal to amend the transitional provisions of Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017/746 on.

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