Sep 30, 2021
Canada
Health Canada, the country’s regulating authority in the sphere of healthcare products, has published a guidance document dedicated to the regulatory requirements for the investigation of reported medical device problems. The document provides additional...
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Sep 7, 2021
Canada
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...
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Sep 7, 2021
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 dedicated to medical device reporting. The document...
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Sep 2, 2021
FDA
The Food and Drug Administration (FDA or the Agency), the US regulating authority in the sphere of medical devices, has published a guidance document dedicated to medical device reporting intended to provide medical device manufacturers with additional clarifications...
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