Predictable, Safe And Business Aware: UK Medtech's Regulatory Wishlist
UK medtech stakeholders face a year of regulatory decision making on MMD Act secondary legislation and the UKCA marking
Executive Summary
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.
You may also be interested in...
UK Regulator Issues More Device Registration Details
Updated MHRA guidance lists the details manufacturers must provide when registering devices in the UK.
New AdvaMed Board Chair To Make Military Veteran Recruitment A Priority
A former Army ranger, Michael Minogue wants to help military veterans transition into and gain employment opportunities in the medtech industry.
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.