United Kingdom
The present article is dedicated to the UK WEEE regulatory requirements the parties involved should comply with.
European Union
The article provides a general overview of the UK regulatory framework for medical devices.
Great Britain
The article highlights the key points related to the UK regulatory framework for clinical investigations involving medical devices.
Great Britain
The article describes in detail the approach the UK authority intends to apply when implementing amendments to the existing legal framework.
Great Britain
The new article provides additional clarifications regarding the upcoming changes to the UK regulatory framework.
MHRA
The article provides an overview of the current reporting requirements for healthcare products allowed to be used for clinical trials.
