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FDA Industry Systems FDA Industry Systems (FIS) was created to facilitate making submissions to the U S Food and Drug Administration (FDA), including registrations, listings, and other notifications
FDA industry systems - Accounts management To make submissions to FDA (e g , Food Facility Registration, Prior Notice, etc ) you must first create an account Select "Create New Account" towards the bottom left side of this page
CDER OMQ e-Portal FURLS User Guide - Food and Drug Administration Once the account has been created, an FDA Administrator will review your account details and grant access to FURLS Once the account has been approved, you will be able to log into the Online Account Administration (OAA) system and gain access to FURLS
FDA Industry Systems - PRA PRAStaff@fda hhs gov An agency may not conduct or sponsor, and a person is not required to respond to, a collection of information unless it displays a currently valid OMB number
OCARUserGuide - Food and Drug Administration FDA will require the IPR’s name and email address to provide access to the portal FDA will send a system-generated email notification to the IPR, including a FURLS OAA account link and a verification code (Figure 2 1)
Confirm U. S. Agent Notification Receipt - Food and Drug Administration The U S Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) received Registration and Listing information identifying you as the U S Agent for the foreign medical device establishment
FECV - FURLS Export Certificate Validator - Food and Drug Administration This Portal allows validation of export certificates issued by the Food and Drug Administration CVM eCATS (CVM Export Certification Application and Tracking System) issued by the Center for Veterinary Medicine Search CVM-Issued Export Certificates