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Tip of the Week: What is FDA’s Temporary Flexibility Policy for Labeling?
Tip of the Week: What is FDA’s Temporary Flexibility Policy for Labeling?
FDA recognizes that supply chain disruptions, including ingredient shortages, can lead to stoppages in food production. Some manufacturers may choose to substitute an alternate ingredient in an effort to continue producing. Because alternate ingredients may differ slightly in composition, substituting ingredients can be a challenge, as this change would most likely not be reflected in the ingredient list on the package label.
1998 Views
Resources from the March 30 “Food Safety and COVID-19: What Businesses Need to Know” Webinar
Resources from the March 30 “Food Safety and COVID-19: What Businesses Need to Know” Webinar
On March 30, we hosted our “Food Safety and COVID-19: What Businesses Need to Know” webinar. Below, you will find links to resources that may be useful in addressing your food safety needs in relation to COVID-19. As you have additional questions, please email us at info@aibinternational.com and we’ll provide you with the right expertise.
1587 Views
FDA Has Started to Enforce the New IA Rule. So Now What?
FDA Has Started to Enforce the New IA Rule. So Now What?
While the FDA began enforcing its new FSMA intentional adulteration rule on March 1, the rule actually went into effect months earlier. Earl Arnold, manager of food defense/FSMA, operations and quality assurance at AIB International, said the FDA agreed to delay inspections until this month to allow for more complete training materials.
1509 Views
4 Highlights from FDA’s Supplemental Draft Guidance for the Intentional Adulteration Rule
4 Highlights from FDA’s Supplemental Draft Guidance for the Intentional Adulteration Rule
The FDA just released the Supplemental Draft Guidance for Industry: Mitigation Strategies to Protect Food Against Intentional Adulteration. This third and final portion adds to the previously published draft guidance with chapters covering food defense corrective actions, food defense verification, reanalysis, and recordkeeping. It also includes appendices on FDA’s mitigation strategies database and how businesses can determine Small and Very Small Businesses status under the IA rule.
737 Views
Where Do Service Dogs Go in Food Processing Plants?
Where Do Service Dogs Go in Food Processing Plants?
AIB International Director of Quality Assurance, Bonnie Biegel, explores the challenges of including service dogs in the food industry.
1755 Views
Tip of the Week: Defining “Best if Used By” Phrase
Tip of the Week: Defining “Best if Used By” Phrase
Reduction of food waste, quality-based date labeling, and best practices on food storage are three topics the FDA is looking at to raise awareness and inform food producers.
1293 Views
Final Guidance Issued for the Declaration of Single-Ingredient Packaged Sugar Products and for Certain Cranberry Products
Final Guidance Issued for the Declaration of Single-Ingredient Packaged Sugar Products and for Certain Cranberry Products
Many manufacturers of single-ingredient sugar products and of cranberry products have been waiting on this finalized guidance to make the changes to their nutrition facts panels for compliance with the regulations issued in May 2016. Here we breakdown all the information you need.
984 Views
Tip of the Week: What is the "seek & destroy" approach in an environmental monitoring program?
Tip of the Week: What is the
How does a food facility incorporate the finding and fixing of potential sources of contamination (e.g., niches) before food safety is compromised?
1500 Views
Tip of the Week: Intentional Adulteration Rule: FDA Clarifies Training Requirements
Tip of the Week: Intentional Adulteration Rule: FDA Clarifies Training Requirements
The draft document is the latest communication in the ongoing IA rule discussion leading up to the July 2019 deadline for those other than small and very small businesses defined by the FDA. A total of 65 new pages were added and reviewed by AIB International’s Food Defense Consultant, Earl Arnold.
1955 Views
Preparing for impending FSMA regulatory deadlines
Preparing for impending FSMA regulatory deadlines
The Center for Food Safety and Applied Nutrition estimates a turnover rate of 33 percent for FDA-regulated facilities. To ensure that personnel perform their jobs well, appropriate training and maintaining food defense records, corrective actions, and verification activities must be evaluated.
1283 Views
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