HSA Revised Guidance on Medical Device Product Registration: Overview
The article outlines the key points associated with registering healthcare products under the existing legal framework.
The article outlines the key points associated with registering healthcare products under the existing legal framework.
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.
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.
The article provides an overview of the trend report template issued by the Swiss regulating authority.
The new article highlights the aspects related to the device description to be included in premarket notification submissions under the respective legal framework.
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