
MHRA Guidance on MD Regulations
The article provides a general overview of the UK regulatory framework for medical devices.
The article provides a general overview of the UK regulatory framework for medical devices.
The article highlights the key points related to the UK regulatory framework for clinical investigations involving medical devices.
The article describes in detail the approach the UK authority intends to apply when implementing amendments to the existing legal framework.
The new article provides additional clarifications regarding the upcoming changes to the UK regulatory framework.
The new article describes in detail certain specific aspects associated with registrations necessary to make submissions associated with healthcare products.
The article provides a general overview of the regulatory framework applicable to certain innovative products intended to be marketed and used in the UK.