UK Medicines And Medical Devices Act 2021 Passed Into Law
The duties of the new commissioner for patient safety have been prioritized in the UK’s Medicines and Medical Devices bill, which has been given Royal Assent.
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The UK’s new medical device registration system, one element of the post-Brexit transition being overseen by the MHRA, is going more or less to plan in the early stages of the standstill period.
In the three months since Brexit, UK medtech stakeholders have seen the beginnings of new regulations, foreign trade plans being put in place, and perhaps new perceptions of medtech’s value.
A public consultation on the UKCA marking for medtech products is anticipated later in the year. Medtech industry representatives are part of the UK regulator’s advisory team.