FDA
The new article provides further clarifications regarding requests for information as provided under the existing legal framework.
Medsafe
The article highlights the key points related to the regulatory requirements for clinical trials in New Zealand.
Australia
The new article describes in detail the regulatory approach to be applied with respect to middleware used for healthcare purposes.
Australia
The new article provides additional clarifications regarding the regulatory approach to be followed with respect to the tools intended to be used for the digitalization of paper-based records used in the healthcare sphere.
Australia
The new article describes additional aspects related to the regulatory status of the products for electronic healthcare records.
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