How does the Food Safety Modernization Act (and specifically Preventive Controls for Human Food) affect your Hazard Analysis Critical Control Point (HACCP), food safety plans and your Quality Control Laboratory?
Some free training material is helpful yet confusing. So you will need to do additional editing and fine-tuning to create documents that comply with regulatory requirements.
The Food and Drug Administra-tion’s time-clock for enforcing the most important FSMA regulation, the “Preventive Controls for Human Foods (PCHF)” started in mid-September 2016. As I write this in early December, it appears that FDA will be training its field investigators and regional milk specialists well past the end of 2016.
It all depends upon your point of view. But one thing is for sure: every dairy plant will be required to have a “qualified individual” who is responsible for
the facility’s FSMA program.
The dairy industry sets an ambitious 80% commitment goal by next year. A dairy processor can implement the practices with paper and pencil in just a few minutes a day.
September 12, 2013
The Innovation Center for U.S. Dairy released voluntary best practices for enhanced dairy traceability. The practices were designed to increase global competitiveness, help satisfy future requirements of FSMA and quickly isolate products in the event of a safety issue.
The agency extends the public comment period 60 days for proposed rules on preventive controls for human food, produce safety.
August 8, 2013
FDA today issued Federal Register notices to extend the comment periods on the proposed rules for Current Good Manufacturing Practice and Hazard Analysis and Risk-Based Preventive Controls for Human Food and Standards for the Growing, Harvesting, Packing, and Holding of Produce for Human Consumption 60 days until November 15, 2013. This is the second and final extension of the comment period for these two rules. The extension of the comment period also applies to the information collection provisions associated with the proposed rules.
A new survey by iRely shows that most companies are still unaware of how the changes will affect them
May 8, 2013
Most process manufacturing organizations are unaware or uncertain at how the stricter regulations will affect their production processes. This is the finding of a new study of food and beverage manufacturing professionals across the county. Conducted by iRely, a leading provider of process manufacturing and commodity trading software, survey data confirms that while food & beverage manufacturing leaders are mostly aware of the new requirements, they are still getting up to speed with the necessary changes.
Food defense is way beyond food safety. Search the FDA’s mitigation strategies database for ideas how to improve security around a blend tank, pasteurizer or other equipment.
For the last 10 years, I have been working closely with federal and state government officials on the prevention of intentional contamination of food, or what is known in our government as food defense.
The Listeriosis risk assessment is a joint effort between FDA and Health Canada. FDA seeks FSMA comments at meetings in Illinois, Oregon.
February 12, 2013
The U.S. Food and Drug Administration (FDA) is announcing two additional public meetings on the Food Safety Modernization Act (FSMA): Proposed Rules for Produce Safety and for the Preventive Controls for Human Food. Last week the agency announced a draft quantitative assessment of the risk of listeriosis from soft-ripened cheese consumption in the United States and Canada. The risk assessment is a joint effort between FDA and Health Canada.
The workshops are in Rosemont, Ill., at Dairy Management Inc.
October 29, 2012
The Center for Food Safety & Regulatory Solutions (CFSRS) with Dairy Foods columnist Allen Sayler as the managing partner, is holding training workshops this month.
Facilities can register online, via mail or fax. FDA encourages online registration.
October 20, 2012
The U.S. Food and Drug Administration (FDA) issued further information and guidance regarding registration requirements for domestic and foreign manufacturers, processors, packers or holders of food for human or animal consumption based on changes made by the FDA Food Safety Modernization Act (FSMA) to the Federal Food, Drug, and Cosmetic Act (FD&C Ac