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Senator Collins Announces FDA To Hold Listening Session In Maine On Proposed Food Safety Rules

WASHINGTON, D.C.-U.S. Senator Susan Collins, a member of the Senate Agriculture Appropriations Subcommittee, today announced that the Food and Drug Administration (FDA) will hold a listening session in Maine regarding the Food Safety Modernization Act (FSMA) on Monday, August 19th. The meeting will be held at the Augusta Armory at 179 Western Avenue.

Last week, Senator Collins received a commitment from Mike Taylor, Deputy Commissioner for Foods and Veterinary Medicine at FDA to hold a listening session in Maine to discuss implementation of the FSMA rules.

"After meeting with the FDA Deputy Commissioner, I am pleased that FDA has agreed to my request to work with the Maine Department of Agriculture to hold a listening session in Maine in August," said Senator Collins. "This will be an opportunity for Maine stakeholders, such as organic farmers and apple growers, to better understand the proposed rules. Food safety provides valuable consumer protections and stakeholder feedback is essential for helping ensure that the rules meet the needs of all New England producers without imposing onerous regulations, especially on small farms and processors."

Background:

In May, Senator Collins joined several Senate and House colleagues in urging FDA to hold a public hearing and listening session in New England on the FSMA proposed rules. The letter pointed out the substantial financial and regulatory burdens that could be imposed by some provisions in the rule on New England's small farms and value-added on-farm enterprises. On July 9, FDA responded to the May letter and indicated the agency's intent to conduct a series of listening sessions in New England later this summer. At Senator Collins' urging, FDA has agreed to host a listening session in Maine in August and will work with Maine Agriculture Commissioner Walt Whitcomb to determine the exact date and location.

In January 2013, FDA proposed two FSMA rules: preventive controls for human food and standards for produce safety. FDA extended the public comment period through September 16, 2013.