Great Britain
The new article describes in detail the new regulatory policy for in vitro diagnostic medical devices as suggested by the UK authority.
Great Britain
The article highlights the key points associated with the concept of common specification requirements for certain products allowed to be marketed and used in the UK.
Great Britain
The new article describes in detail certain specific aspects associated with registrations necessary to make submissions associated with healthcare products.
Great Britain
The article highlights the key points related to the registration process to be completed by interested parties to be able to make submissions via the e-submission system implemented in the UK.
AIaMD
The article provides a general overview of the regulatory framework applicable to certain innovative products intended to be marketed and used in the UK.
Great Britain
The new article provides an overview of the regulatory approach to medical devices allowed for marketing and use in the United Kingdom.
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