Status of CE and UKCA marking use in the United Kingdom
Since Brexit came into force in 2021, the legislation of the European Union does not…
Use of CE marking in the United Kingdom: new extensions for manufacturers
The CE marking proves that goods on the EU market meet the applicable regulatory requirements.…
First UK Approved Body since Brexit to be designated by the MHRA
One more step towards a strong UKCA regulatory framework for Medical After the withdrawal of…
Nutrition and health claims register in the UK after Brexit: are EU claims valid also in the UK?
With Brexit, Great Britain adopted new legislation, and their laws might differ from the European…
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…
The future of the UK Medical Devices regulatory regime
An insight on the Medicines and Healthcare products Regulatory Agency Delivery Plan 2021-2023 and the…
Update on technical specification for transparent face masks
Since the beginning of the pandemic of Covid-19, the usage of face mask has increased,…
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…
How does Brexit affect the commercialization of your cosmetic products?
Regardless the outcome of the ongoing EU trade negotiations, Brexit will imply certain consequences for…