SFDA Guidance on Medical Devices Samples Collection: Overview
The article provides an overview of the regulatory framework for sample collection.
The article provides an overview of the regulatory framework for sample collection.
The new article highlights the aspects related to the classification rules applicable to specific categories of healthcare products.
The article provides a general overview of the classification framework for medical devices.
The new article highlights the key points related to the regulatory requirements associated with changes to the materials used in medical devices. Also, it outlines the scope of information to be included in the medical device change form to be submitted by the...
The new article highlights the aspects related to the changes to the design of a medical device and the potential impact thereof. Table of Contents The Saudi Food and Drug Administration (SFDA), a county’s regulatory agency in the sphere of healthcare products, has...