UK Reveals How To Access Fast-Track Approval Of Devices During COVID-19 Outbreak

 
• By Amanda Maxwell

How to quickly get non-CE-marked medical device onto the UK market.

Fast_Track

The UK medtech regulator is expecting to receive a high volume of applications from manufacturers of products intended to address the COVID-19 crisis but which haven’t demonstrated compliance with its Medical Device Regulations 2002. The UK Medical Device Regulations 2002 transpose the EU’s Medical Devices Directive (MDD).

“We will prioritise applications based on the needs of the healthcare providers to increase the supply of critical devices and...

Read the full article – start your free trial today!

Join thousands of industry professionals who rely on Medtech Insight for daily insights

  • Start your 7-day free trial
  • Explore trusted news, analysis, and insights
  • Access comprehensive global coverage
  • Enjoy instant access – no credit card required
Start Free Trial

Already a subscriber?

More from Europe

More from Geography

MHRA Opens Second AI Airlock Program For Applications

 
• By Natasha Barrow

"The AI Airlock program creates a supervised testing ground where novel technologies and challenge areas can be safely investigated," said James Pound, MHRA interim executive director of innovation and compliance.

Stealth Mode AI Imaging Startup Faction Imaging Raises $10M

 
• By Natasha Barrow

Faction Imaging has come out of stealth mode following six years of research and development studying medical imaging workflows in India, Japan and the US.

Medtronic Announces Collaboration To Create A ‘New Era’ in Surgical Training

 
• By Brian Bossetta

Medtronic is teaming up with IRCAD North America to build high-tech training and education experiences for surgeons and medical professionals in cardiovascular, neuroscience, and minimally invasive surgical specialties. The move could also further position Medtronic to seize on the growing robotics