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Nov 12, 20222 min read

USFDA MD Guidance: Referencing “Device” and “Counterfeit Device”

According to the US Food and Drug Administration's draft guidance, the definition of a device has been updated according to the...

Jun 11, 20211 min read

FDA’s New Draft Guidances on Device Postmarket Surveillance – For Comments

The US Food and Drug Administration (FDA) has issued draft guidance to help Medical Device Manufacturers comply with postmarket...