SFDA Guidance on Innovative Medical Devices: Overview
The article outlines the basics of the regulatory framework for innovative medical devices.
The article outlines the basics of the regulatory framework for innovative medical devices.
The article outlines the key aspects to be covered by the labeling used for contact lenses.
The article highlights the critical points associated with the regulatory framework for surgical sutures intended to be marketed and used in Saudi Arabia.
The article provides a general overview of the regulatory requirements for medical devices developed by healthcare institutions to meet their internal needs.
The new article highlights the critical points associated with the concept of intended use and clarifies the approach to be applied concerning risks associated with in-house medical devices.
The new article describes in detail the regulatory approach to be followed concerning the manufacturing process, post-market surveillance, and other aspects.
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