Australia
The new article provides an in-depth overview of the problems identified and solutions proposed by the authority, together with the questions to be answered by the key stakeholders.
SFDA
The article provides an overview of the regulatory framework for sample collection.
FDA
The article provides a brief overview of the approach to be followed for the reports related to studies and reports associated with it.
HSA
The new article highlights specific points related to medical device registration in Singapore under the existing legal framework.
HSA
The new article describes in detail the approach to be followed when applying for registration and marketing approval for Class A and B medical devices.
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