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 FDA Reportable Food Registry 9/4/09
To Our Valued Customers and Suppliers:
On September 27, 2007, the President signed into law the Food and Drug Administration Amendments Act of 2007 (FDAAA). This law amends the Federal Food, Drug, and Cosmetic Act (FD&C Act) by creating a new section referred to as 417, Reportable Food Registry (RFR).
The FDA RFR electronic portal will be implemented as a part of FDA's new electronic system for collecting, submitting and processing adverse event reports and other safety information for all FDA-regulated products. The FDA RFR electronic portal will be listed and available on the FDA.GOV website on September 8, 2009. All food manufacturers must comply with the requirements of the Reportable Food Registry (Section 417 of the FD&C Act) on September 8, 2009 The FDA RFR electronic portal will be accessible through a link on the FDA.GOV web site home page (http://www.fda.gov) under the heading "Report a Problem." Alternatively, you will be able to access the FDA RFR electronic portal directly by entering the following URL into your browser: The FDA RFR electronic portal shall be used for a food product (other than infant formula) where it is deemed that there is a reasonable probability that the use of, or exposure to, such article of food will cause serious adverse health consequences or death to humans or animals. Thus, on September 8, 2009, Rich Products Corporation will comply with all requirements mandated by the FDA RFR. Rich Products Corporation highly recommends that our valued customers and suppliers become familiar with section 417, Reportable Food Registry (RFR) to fully understand the potential impact to your organization’s resources. FDA guidance document can be found at:
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