FDA Food Safety Modernization Act: Proposed Rules to Establish Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption and for Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food Public Meeting
Purpose: To discuss the proposed rules to establish standards for growing, harvesting, packing and holding of produce for human consumption (the produce safety proposed rule) and for current good manufacturing practice and hazard analysis and risk-based preventive controls for human food (the preventive controls proposed rule), which are the first of several proposed rules that would establish the foundation of, and central framework for, the modern food safety system envisioned by Congress in the FDA Food Safety Modernization Act (FSMA).
Public Meeting: Chicago, Illinois
| Date: | March 11, 2013: 8:30 am — 5:00 pm March 12, 2013: 8:30 am — 12:00 pm Onsite Registration: 8:00 am — 8:30 am |
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| Location: | The Westin Michigan Avenue 909 North Michigan Avenue Chicago, IL 60611 | |
Please note the following important dates: | ||
| February 21, 2013: | Closing Date for Request to Make Oral Comment Closing Date to Request Special Accommodation due to a Disability | |
| March 1, 2013: | Closing Date for Advance Registration | |
| May 16, 2013: | Closing date to submit either electronic or written comments to FDA's Division of Dockets Management. Docket Numbers: FDA-2011-N-0920 and FDA-2011-N-0921 | |
Public Meeting: Portland, Oregon
| Date: | March 27, 2013: 8:30 am — 5:00 pm March 28, 2013: 8:30 am — 12:00 pm Onsite Registration: 8:00 am — 8:30 am |
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| Location: | Crowne Plaza Portland Downtown Convention Center 1441 NE 2nd Avenue Portland, OR 97232 | |
Please note the following important dates: | ||
| March 8, 2013: | Closing Date for Request to Make Oral Comment Closing Date to Request Special Accommodation due to a Disability | |
| March 18, 2013: | Closing Date for Advance Registration | |
| May 16, 2013: | Closing date to submit either electronic or written comments to FDA's Division of Dockets Management. Docket Numbers: FDA-2011-N-0920 and FDA-2011-N-0921 | |