FDA Record Access
Record access guidance allows the FDA access to records including: manufacturing, raw materials (ingredients and packaging) receipts, product distribution, testing, recalls and reportable foods, customer distribution as well as complaints and adverse events in all registered facilities. If requested these records must be provided to the FDA within 24 hours. Failure to do so can result in the suspension of a facility’s registration, recalls, injunctions or product seizures.
Progress on FSMA
Biennial Registration for all facilities opened on October 22, 2012 and all renewals must be submitted by December 31, 2012. Failure to re-register through this process may result in suspension of registration, as of January 1, 2013. Facilities whose registration is suspended cannot ship products into the USA, nor can they ship goods within the country. Other FSMA rules, guidance documents and reports (http://www.fda.gov/
• Publication of three final rules in the Federal Register.
• Publication of 11 draft and final guidance documents in the Federal Register with a further 2 in clearance.
• Completion and submission of five reports to Congress.
• Publication of notices on state and local food defense capacity and the implementation of FSMA re-inspection fees.
• Anti-smuggling strategy published jointly with the Department of Homeland Security.
• Product tracing pilot studies conducted.
• Memorandum of Understanding signed with the US Department of Agriculture to establish an FSMA implementation grant program for small-scale produce growers.
In addition, the FDA has made very substantial progress on other major FSMA deliverables, including:
• Four major frameworks for proposed rules and accompanying regulatory impact analyses are now under review at the Office of Management and Budget (OMB), covering: preventive control standards for human and animal food facilities; produce safety standards; foreign supplier verification requirements for importers.
• Proposed rules to establish an accredited third party certification program and transport safety standards are close to completion within the FDA.
• An advance notice of proposed rulemaking on intentional adulteration drafted and close to completion within the FDA (1).
While the OMB is still reviewing three major rules, a further two are nearing completion and the FDA has delivered:
• Record Access Guidance and Interim Rule – February 2012 (2).
• Report to Congress on US FDA Foreign Offices – February 2012.
• Sprout Safety Alliance Development–
• High Risk Facility Definition – March 2012.
• More Data Elements for the Reportable Food Registry – June 2012.
• 2012 Report to US Congress – August 2012.
• Increase Category information for Registration – August 2012.
• Biennial Facility Registration – October 2012 (3).
On 4 January 2013, the US FDA issued the proposed preventive controls for human food and the produce safety standards. US FDA will receive comments to these proposals until 16 May 2013(4).
Some 48 million people (1 in 6 Americans) get sick, 128,000 are hospitalized, and 3,000 die each year from foodborne diseases, according to recent data from the Centers for Disease Control and Prevention. The FSMA will better protect public health by strengthening existing food safety systems and proving oversight of producer and processor compliance.
About SGS Food Safety Services
SGS is committed to keeping you informed of regulatory news and developments. Leveraging a global network of laboratories and food experts, SGS provides a comprehensive range of food safety and quality solutions (http://www.sgs.com/
For more details on US FSMA and SGS Food services please contact the local SGS expert.
(1) Progress on FSMA, Changes within the FDA Foods Program, and on Partnerships (http://www.fda.gov/
(2) Record Access (http://www.gpo.gov/
(3) Registration (http://www.fda.gov/
(4) Preventive Control for Human Foods (http://www.gpo.gov/
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