Just two months to go before crucial medtech discussion roadmap is revealed
This article was originally published in Clinica
It will soon become clear which issues EU medical device regulatory experts believe will need addressing the most urgently in order to drive the future of the medtech sector.
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Following hot on the heels of its Rapidly Manufactured Ventilator Specification document, the UK’s regulator has issued another speedy regulatory permit for fast production of respiratory assist devices.
The UK is taking measures to increase its ventilator stock from 8,000 to some 30,000, but it will take time to make them available. Many are asking whether the government really rejected EU help, which could have brought relief sooner, because of Brexit.
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