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EU Restricts Coronavirus PPE Equipment Exports

 
• By Ashley Yeo

The rapidly escalating COVID-19 crisis in Europe – now the global 'epicenter' of coronavirus infections  ̶   has forced the European Commission to put in place export controls on personal protective equipment.

EU

The European Commission has issued an implementing regulation restricting the export of major types of personal protective equipment (PPE).

Dated 14 March, the regulation (2020/402) makes the export outside the EU of protective spectacles and visors, mouth-nose protection equipment, face shields and protective gowns and suits subject to authorization,...

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Medtechs Eye German Health Minister Switch As Governing Parties Reach Coalition Agreement

 
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More from Europe

Commission’s Flora Giorgio Says Simplification And Safety Are Key In Evolving EU Regs

 
• By Amanda Maxwell

Predictability, proportionality, stability, harmonization and simplification offer the right way forward to address the challenging unintended effects of the EU medical device regulations, the European Commission’s head of devices tells the EU’s largest annual medtech conference.

Swiss Medtechs Advised To Work On US Tariff Mitigation Strategies

 
• By Ashley Yeo

The US’ 90-day suspension of higher “reciprocal tariffs” will expire on 9 July, raising fears that the 31% tariff rate on Swiss medtech and other goods exported to the US might make a comeback. While the tariff situation changes on an almost daily basis, medtechs should forearm for any eventually, say local business organizations.

Inclusive By Design: UK Invites Sponsors To Submit Trial Diversity Plans

 
• By Vibha Sharma

The UK has issued clearer guidance to help drug and medical device sponsors demonstrate how they intend to include a diverse and relevant range of participants in their clinical trials.