food and drug administration modernization act
-
-
Agency meets critical milestones in Food Safety Modernization Act
SILVER SPRING, Md., July 5, 2011 /PRNewswire-USNewswire/ -- The U.S. Food and Drug Administration today announced that it has completed two tasks required by the new Food Safety Modernization Act (FSMA). FDA has issued an anti-smuggling strategy, and issued draft guidance clarifying agency expectations on new dietary .
-
The Food and Drug Administration (FDA) is announcing a publication containing modifications the Agency is making to the list of standards FDA recognizes for use in premarket reviews (FDA recognized consensus standards). This publication, entitled ``Modifications to the List of Recognized Standards, Recognition List Number: 028'' (Recognition List Number: 028), will assist manufacturers who elect to declare conformity with consensus standards to meet certain requirements for medical devices.
-
-
The Food and Drug Administration has released two new regulations pursuant to the Food Safety Modernization Act, which increased the agency's authority to recall unsafe foods.
The Act also requires food producers to give FDA officials access to records in the event of a food-borne illness outbreak, and endows the agency with the power to suspend the registration of a food facility for causing serious adverse health consequences or death to humans or animals. President Barack Obama signed the measure into law in January.
-
-
PATERSON -- A new federal law, signed by President Obama last month, will require food producers to map the exact DNA makeup of whatever they manufacture and sell to grocery stores, so that regulators can better trace contaminated ingredients during a recall. That new mandate could mean an opportunity for a company in Riverdale.
The Food Safety Modernization Act requires the Food and Drug Administration to establish a product tracing system, which, in turn, could force food companies to better track the supply-chain movement of each ingredient used in every batch. Bakers in New Jersey, for example, will need to document which sack of salt they used to make the last round of semolina bread, and more important, which stores and restaurants received those loaves.
-
-
The Food and Drug Administration (FDA) is announcing that a proposed collection of information has been submitted to the Office of Management and Budget (OMB) for review and clearance under the Paperwork Reduction Act of 1995 (PRA). The proposed collection of information concerns a guidance document that outlines the criteria and the process through which firms may request a reduction of fees based on severe economic hardship of the FDA Food Safety Modernization Act (FSMA) reinspection and recall user fees that are mandated by the Federal Food, Drug, and Cosmetic Act (the FD&C Act).
-