Saudi Arabia
The article highlights the critical points associated with the regulatory framework for surgical sutures intended to be marketed and used in Saudi Arabia.
Saudi Arabia
The article provides a general overview of the regulatory requirements for medical devices developed by healthcare institutions to meet their internal needs.
Australia
The article provides an overview of the legal framework for labeling requirements applicable to medical devices intended to be marketed and used in Australia.
Canada
The new article describes specific types of changes to medical devices in detail and outlines the critical points related to the regulatory status thereof.
FDA
The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere of healthcare products, has published a guidance document on reprocessing medical devices in healthcare settings. The document highlights the most important aspects...
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