FDA announces availability of e-submission process for requesting CDRH export certificates…

FDA announces availability of e-submission process for requesting CDRH export certificates…

On January 22, FDA announced via Federal Register the availability of an electronic submission process for requesting export certificates for products regulated by FDA’s Center for Devices and Radiological Health (CDRH). The e-process is aimed to help meet certain requirements set out by the FDA Export Reform and Enhancement Act of 1996 and other FDA requirements.

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