A quick dive into GMDN and UDI codes
Global Medical Devices Nomenclature (GMDN) is an integral part of the MHRA MD and IVD…
The future regulations of medical devices in the United Kingdom
Following Brexit, many changes have been introduced to how medical and in vitro diagnostic devices…
Updates to the UK Toys & Cosmetics Regulations notified to WTO
On April 13, 2022, the United Kingdom notified the draft “The Toys and Cosmetic Products…
UK and Brexit: towards new Regulations for IVD medical devices
In May 2017, the European Union introduced two new Regulations for medical devices, the Medical…
Expired certificate in the UK: implication and actions to take
In order to sell medical devices on the UK market, the manufacturer shall register their…
All antigen and molecular COVID tests will need to pass validation
On 28 July 2021, the UK government made it a legal requirement to seek validation…
The UK market after Brexit – The end of grace periods for registering your MDD&IVDs and Cosmetics is approaching quickly
Manufacturers of medical devices, IVDS, and cosmetics, are you aware of the new UK requirements…
UK’s new dedicated Yellow Card reporting site
The UK is determined to display full information for users of medical devices, and it…
What are the implications of Brexit for Medical Device Companies up to December 31, 2020?
The Irish Health Products Regulatory Authority (HPRA) has recently issued a brief explanation of the…