Europe
The new article highlights aspects related to changes to medical device registration and also describes in detail the public register of medical device manufacturers. Table of Contents The Medicines and Healthcare Products Regulatory Agency (MHRA), the UK regulating...
Europe
The new article addresses the aspects related to special types of products, as well as to the online registration system to be used and the approach to be applied when renewing the registration. Table of Contents The Medicines and Healthcare products Regulatory Agency...
Europe
The new article highlights aspects related to the information to be included in the submission in order to ensure its completeness. Table of Contents The Medicines and Healthcare Products Regulatory Agency (MHRA), the UK regulating authority in the sphere of medical...
Europe
The article provides a brief overview of the way medical devices should be registered when placed on the UK market. Table of Contents The Medicines and Healthcare Products Regulatory Agency (MHRA), the UK regulating authority in the sphere of healthcare products, has...
Europe
The new article highlights the aspects related to the general essential requirements, as well as the ones related to the design of medical devices to be followed in order for the latter to be allowed for marketing and use in the United Kingdom. Table of Contents The...
Europe
The article provides a brief overview of an updated guidance document issued by the UK regulating authority with respect to software products subject to regulation as medical devices. Table of Contents The Medicines & Healthcare Products Regulatory Agency (MHRA),...
