GRTPNZ
The new article provides further clarifications on certain specific aspects associated with the regulatory requirements healthcare products, including medicines and medical devices, should comply with in order to be allowed for marketing and use in New Zealand.
Medsafe
The new article explains the approach to be applied with respect to different categories of healthcare products based on specific criteria.
BfArM
The article provides an overview of the authorization process for clinical trials involving medical devices to be conducted in Germany.
Great Britain
The new article describes in detail certain specific aspects associated with registrations necessary to make submissions associated with healthcare products.
FDA
The article provides a brief overview of the regulatory approach to be applied with respect to certain tests intended to be used in the context of an emergency.
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