Swissmedic Information Sheet on Combination Studies: Reporting
The new article outlines the reporting requirements to be followed by the parties responsible for clinical investigations conducted in Switzerland.
The new article outlines the reporting requirements to be followed by the parties responsible for clinical investigations conducted in Switzerland.
Health Canada, the country’s regulating authority in the sphere of healthcare products, has published a guidance document dedicated to medical device recalls. The document provides guidelines to be followed by medical device manufacturers with regard to their products...
The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere of healthcare products, has published a guidance document dedicated to medical device reporting. The document...
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