GRTPNZ
The article highlights the key points related to the regulatory framework for healthcare products in New Zealand
GRTPNZ
The new article describes in detail the key elements of the regulatory system for healthcare products.
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.
EU MDR/IVDR
The European Medicines Agency (EMA) has published guidelines dedicated to the quality documentation to be provided for medicinal products intended for use with medical devices. The present article addresses matters related to medicinal products with co-packaged or...
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