INDUSTRY EXPERT ARTICLES

The UK will continue with the UK Medical Devices Regulations 2002 (S.I. 2002/618) (UK MDR), as amended, and by the 30th of June 2023, manufacturers will need to follow the UK Conformity Assessment process and place the UKCA mark on their medical devices, as CE marked medical devices will stop being recognised in Great Britain (England, Scotland and Wales).

If the nation has learned anything from the Covid-19 crisis, it’s that advance planning in safety preparedness is vital to our ability to respond to emergencies, whether they’re viral, violent, or otherwise.

Clinical trials are the most efficient and primary technique researchers have at their disposal when trying to understand whether a drug, treatment, or device is safe & effective in humans. Get all the tips!

As a burn and trauma surgeon for the U.S. Army Institute of Surgical Research Burn Center, I’ve personally seen the powerful advantages of SILVERLON dressing in treating hundreds of burn injuries — including during my three combat deployments.