Malaysia
The article provides a general overview of grouping requirements applicable in Malaysia.
Malaysia
The article provides a general overview of grouping requirements applicable in Malaysia.
Serbia
The article describes in detail the approach to be applied when requesting changes to the existing medical device registration.
SFDA
The article provides an overview of the regulatory framework for sample collection.
United States
The highlights the aspects to be taken into consideration in order to ensure the real-world data used to support regulatory submissions is relevant and reliable.
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