SFDA Guidance on Biotechnology-Based Medical Devices: Overview
The article provides a general overview of the regulatory approach to be applied concerning biotechnology-based medical devices intended to be marketed and used in Saudi Arabia.
The article provides a general overview of the regulatory approach to be applied concerning biotechnology-based medical devices intended to be marketed and used in Saudi Arabia.
This article highlights the critical points related to the procedures to be followed by medical device manufacturers and other parties involved in case changes to medical devices allowed for marketing and use in Canada.
The article provides a general overview of the regulatory framework for medical devices with measuring functions.
The new article describes specific types of changes to medical devices in detail and outlines the critical points related to the regulatory status thereof.
The article highlights the critical points related to the concept of significant changes in the context of medical devices allowed for marketing and use in Canada.
The new article describes in detail the regulatory approach to be followed when reviewing the applications related to clinical investigations to be conducted in Pakistan.