MHRA Guidance on Future Regulations: Overview
The article describes in detail the approach the UK authority intends to apply when implementing amendments to the existing legal framework.
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 article provides a general overview of the new regulatory framework for innovative AI-based healthcare products intended to be marketed and used in the UK.
The new article outlines the list of questions raised by the regulating authority in the context of the initiated consultation and also provides definitions of the most important terms and concepts used.
The new article describes in detail the new regulatory policy for in vitro diagnostic medical devices as suggested by the UK authority.
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.