HSA
The new article describes in detail the approach to be followed when applying for registration and marketing approval for Class A and B medical devices.
HSA
The article outlines the key points associated with registering healthcare products under the existing legal framework.
FDA
The new article describes in detail the enforcement policy introduced by the authority and also highlights the key points to be considered in order to comply with it.
FDA
The article provides an overview of the regulatory requirements related to safety in the magnetic resonance environment and highlights the key points to be taken into consideration by medical device manufacturers and other parties involved.
Swissmedic
The article provides an overview of the trend report template issued by the Swiss regulating authority.
