Medsafe Guidelines on the Regulation of Therapeutic Products: Overview
The article highlights the key points related to the regulatory framework for healthcare products in New Zealand
The article highlights the key points related to the regulatory framework for healthcare products in New Zealand
The new article describes in detail the key elements of the regulatory system for healthcare products.
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.
The new article explains the approach to be applied with respect to different categories of healthcare products based on specific criteria.
by Anne, Consultant on RegDesk – Effective from 1 July 2014 Working toward co-ordination with the Australian Therapeutic Goods Administration (TGA) under the ANZTPA agency, the New Zealand regulatory authority Medsafe has revised and published changes to the...