COVID-19, COVID-19… Needless to say, it is everyone’s duty to tackle and eliminate the virus…
Medical Devices
MHRA update to the guidance on the regulatory status of software (including apps) used in the diagnosis, treatment and management of patients with COVID-19
The Medicines and Healthcare products Regulatory Agency (MHRA) is the standalone regulator for medicines and…
What to know about the UKCA marking
On 1 January, 2021, the United Kingdom left the EU Single Market, meaning that goods…
Prosthetic/Orthotic Devices and Ophthalmic products: requirements from the UK MDR
Are you thinking about placing external prostheses and orthoses devices, or even ophthalmic products on…
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…
Guidance: Regulating medical devices from 1st January 2021 in Great Britain, Northern Ireland and the EU
On 1st September, 2020, the Medicines and Healthcare products Regulatory Agency (MHRA) published its latest…
The latest news on the approval process of the UK Medical Device law
The latest news on the approval process of the UK Medical Device law As COVID-19…
Brexit – Last update
With the whole of Europe at expenses of the outcome, the European Parliament is about…
Brexit – Belgian Ministry of Health dedicated website
At expenses of Brexit becoming effective, the Belgian Ministry of Health has provided through its…