From 1 January 2021 the following devices in Great Britain (England, Wales and Scotland) will need to be registered with the MHRA under existing arrangements: Class I medical devices, IVDs, custom-made devices. All other classes of device placed on the Great Britain market will require registration with the MHRA.

Biohermes’s products have been registered in British Medicines and Healthcare Products Regulatory Agency (MHRA), and obtained the certification.

To be a reliable and respected IVD enterprise, Biohermes has put extensive investments in R&D, developing advanced technologies and create more medical value for health and vitality of people all over the world.