Ann M. Begley
- Indexed articles, last 90 days
- 3
- Latest publication
- Sep 30, 2026
- Outlet visibility, for Mondaq
- Top 500K sites
- Earliest in this view
- Aug 19, 2026
Latest articles
FDA Announces Process Improvements Impacting Animal Food Producers (opens the original)
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The U.S. Food and Drug Administration’s (FDA) Center for Veterinary Medicine (CVM) has concluded its two-year evaluation of the animal Food Additive Petition (FAP) and Generally Recognized as Safe (GRAS) Notification review programs and announced a series of process reforms designed to “deliver faster, more predictable outcomes for submitters.” FDA has characterized these changes as “targeted process improvements,” which include implementing earlier review timelines, allowing submitters to provi
UPDATE: Court Sets January 1, 2028 Deadline To Address Key USDA Bioengineered Rule Disclosure Provisions (opens the original)
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Wiley continues to track the U.S. Department of Agriculture’s (USDA) rulemaking efforts in light of Natural Grocers v. Rollins. Building on 2025 and 2026 analysis, below are the latest developments that food manufacturers need to watch closely. The U.S. District Court for the Northern District of California recently issued its remedy order in Natural Grocers v. Rollins, setting a January 1, 2028 deadline to vacate the successfully challenged provisions of the National Bioengineered Food Disclosu
FDA Proposes Mandatory GRAS Notification Framework (opens the original)
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On August 11, 2026, the U.S. Food and Drug Administration (FDA or Agency) published its highly anticipated proposed rulemaking that would fundamentally revise the regulatory framework governing Generally Recognized as Safe (GRAS) determinations for substances used in human and animal food (the Proposed Rule). The Proposed Rule, if finalized, would revise the GRAS regulations in 21 CFR parts 170 and 570 to require mandatory submission of GRAS notices for human and animal food substances claimed t
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