FDA Guidance on De Novo Classification Process: Overview
The article provides a general overview of the regulatory framework for innovative medical devices intended to be marketed and used in the US.
The article provides a general overview of the regulatory framework for innovative medical devices intended to be marketed and used in the US.
The article provides a brief overview of the eSTAR program and the updates thereto recently published by the US authority.
The article provides a general overview of the approach to be followed when applying for a medical device license necessary to place a new product on the market.
The new article highlights the critical points related to the regulatory framework for novel medical devices intended to be marketed and used in the US.
The new article highlights the critical points related to the regulatory framework for novel medical devices intended to be marketed and used in the US.
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