Amino Acids

A group of organic compounds that serve as the building blocks of proteins, regulated as food additives, animal feed materials, and pharmaceutical ingredients across jurisdictions.

Foresight tracks Amino Acids developments and surfaces the alerts most likely to matter before they turn into missed deadlines, recalls, or escalation work.

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Last updated

6 April 2026, 16:06

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Latest Amino Acids alerts

The most recent regulatory and guidance signals tracked by Foresight

USITC Schedules Final Phase of AD/CVD Investigations on L-Lysine From China

The USITC has scheduled the final phase of antidumping and countervailing duty investigations into Chinese animal feed-grade L-lysine, with a hearing set for July 2026. Importers and downstream users should prepare for potential duty orders that could significantly increase the cost of lysine-based feed additives and disrupt existing supply chains.

federalregister.govUnited StatesUnited States

Japan MAFF Amends Pesticides Control Act Ministerial Standards for Phytase-Based Feed Calculations

Japan's MAFF has updated the Pesticides Control Act ministerial standards to align phytase-based feed calculation cross-references with current feed additive regulations, effective March 30, 2026. This technical correction ensures regulatory consistency for compound-feed formulations, requiring manufacturers to update internal compliance documentation and calculation tools.

kanpo.go.jpJapanJapan

EU DG AGRI Convenes Joint Livestock Meeting on Feed Circularity and Feed Additives

EU DG AGRI is convening a high-level meeting on April 29, 2026, to address feed circularity and regulatory hurdles for innovative feed additives. This signals a policy push toward strategic autonomy in feed supply chains and potential streamlining of market access for sustainable agricultural inputs.

ec.europa.euEuropean UnionEuropean Union

EFSA Registers Intake of L-Isoleucine Feed Additive Application (E. coli CGMCC 33723)

EFSA has initiated the assessment of a new application for L-isoleucine produced by E. coli CGMCC 33723 as a feed additive. If authorized, this will expand the available portfolio of bio-based amino acids for animal nutrition, requiring manufacturers to track future EFSA opinions for compliance and market entry.

open.efsa.europa.euEuropean UnionEuropean Union

USITC Schedules Expedited Second Five-Year Antidumping Reviews of Monosodium Glutamate From China and Indonesia

The USITC has initiated expedited sunset reviews of antidumping duty orders on monosodium glutamate (MSG) from China and Indonesia, with a comment deadline of April 8, 2026. Stakeholders should prepare for the probable extension of these trade barriers, as the expedited process typically indicates a high likelihood that existing duties will be upheld.

federalregister.govUnited StatesUnited States

Japan Food Safety Commission Announces 1020th Meeting on Pesticides, Feed Additives and GMO Soybean DBN9004

Japan’s Food Safety Commission is conducting safety reviews for the insecticide Fenmezoditiaz, GMO soybean DBN9004, and various feed additives during its March 2026 plenary. These assessments are critical for market access, as they form the basis for upcoming revisions to food and feed standards and substance approvals.

fsc.go.jpJapanJapan

EU EFSA Registers GM L-Tryptophan Application AP177 Under GM Food And Feed Regulation

EFSA is currently reviewing an application for the authorization of L-tryptophan produced by genetically modified microorganisms under the GM Food and Feed Regulation. This development signals a potential expansion of approved biotech-derived ingredients, requiring food and feed operators to track the assessment outcome for future supply chain diversification.

open.efsa.europa.euEuropean UnionEuropean Union

USDA AMS Proposes National Organic Program National List Changes for Carbon Dioxide, Sodium Nitrate, Meloxicam and Methionine

The USDA is proposing to update the National Organic Program's National List to allow or renew the use of specific substances, including carbon dioxide, sodium nitrate, and meloxicam, with comments due by May 22, 2026. This update modernizes organic production by expanding tools for pest management and animal welfare while streamlining compliance for poultry producers through the removal of specific nutrient limits.

federalregister.govUnited StatesUnited States

EU EFSA Registers Intake of L-Threonine Feed Additive Application for All Animal Species

EFSA has commenced the risk assessment for a new application of L-threonine as a nutritional feed additive for all animal species. Stakeholders should monitor the assessment's progress as it will dictate future market access and compliance requirements for this fermentation-derived amino acid.

open.efsa.europa.euEuropean UnionEuropean Union

US Commerce Issues Preliminary Antidumping Duty Review Results for Methionine From Spain (2023–2024)

The US Department of Commerce has preliminarily established a 7.11% antidumping duty margin for methionine imports from Spain for the 2023–2024 review period. Affected importers should evaluate the impact on cash-deposit requirements and supply chain costs ahead of the final determination expected in July 2026.

federalregister.govUnited StatesUnited States

US Commerce Issues Preliminary LTFV Determination and Extends Provisional Measures on L-Lysine From China

The US has implemented preliminary antidumping duties on animal feed grade L-lysine from China, effective March 6, 2026. With cash deposit rates reaching 142.59%, businesses must immediately evaluate import costs and supply chain resilience before the final determination in July 2026.

federalregister.govUnited StatesUnited StatesChinaChina

EFSA Consults on Authorisation of Guanidinoacetic Acid as Zootechnical Feed Additive for Chickens and Pigs

EFSA is consulting on the authorization of guanidinoacetic acid as a zootechnical feed additive for poultry and swine through March 16, 2026. Approval would expand the substance's legal use in the EU, requiring feed manufacturers to integrate new zootechnical specifications into their compliance and production planning.

open.efsa.europa.euEuropean UnionEuropean Union

US Commerce Finalises Changed Circumstances Review of Antidumping Order on Glycine From China

The US Department of Commerce has finalized its review of glycine antidumping duties, maintaining trade restrictions on imports from Salvi Chemical Industries due to insufficient proof of non-Chinese origin. This decision reinforces strict traceability requirements for chemical supply chains and highlights the ongoing risk of duty exposure for importers unable to verify the origin of raw material inputs.

federalregister.govUnited StatesUnited States

EFSA FEEDAP Panel Opinion on l-Lysine Sulfate Feed Additive (C. glutamicum KCCM 80368) for All Animal Species

EFSA published a positive scientific opinion in March 2026 on the safety and efficacy of l-lysine sulfate produced via fermentation for use as a feed additive. This assessment clears the path for EU market authorization, though businesses must mitigate identified respiratory and skin sensitization risks for personnel handling the additive.

efsa.onlinelibrary.wiley.comEuropean UnionEuropean Union

EU EFSA Updates Novel Food Application For Gamma-Aminobutyric Acid (GABA)

EFSA has initiated the safety assessment of Gamma-Aminobutyric Acid (GABA) for potential authorization as a novel food in the EU. A successful application will open new market access for functional food and supplement products, contingent on meeting specific safety and purity standards.

open.efsa.europa.euEuropean UnionEuropean Union

Korea MFDS Outlines 2027 Periodic Re-evaluation Programme For Health Functional Food Ingredients

South Korea’s MFDS has announced 31 functional ingredients, including amino acids and botanicals, for its 2027 periodic safety and efficacy re-evaluation. Recognition holders should prepare updated substantiation data by late 2026 to mitigate risks of restricted usage, revised health claims, or potential market withdrawal.

mfds.go.krSouth KoreaSouth Korea

Louisiana Prefiles SB253 Limiting Licensing Board Restrictions on Compounded Peptides

Louisiana SB 253 proposes to prevent state licensing boards from restricting the prescription of compounded peptides sourced from FDA-registered facilities, effective August 2026. This measure protects market access for compounded peptide therapies by limiting state-level regulatory interference, provided federal FDA sourcing and compounding standards are met.

legis.la.govUnited StatesUnited States

Switzerland Proposes OLALA Annex 2 Feed Additive Amendments With 1 June 2026 Entry Into Force

Switzerland has proposed significant updates to its authorized feed additives list (OLALA Annex 2), effective June 1, 2026, including 69 withdrawals and 18 new authorizations. Businesses must review formulations and labeling immediately to manage the phase-out of withdrawn substances and ensure compliance with updated nutritional and sensory additive requirements.

members.wto.orgSwitzerlandSwitzerland

Application for Authorisation of Zinc Chelate of Amino Acids Hydrate and Chromium Chelate of DL‑Methionine as Zootechnical Feed Additive for Poultry for Fattening (Article 4)

EFSA is evaluating the authorization of zinc and chromium chelates as new zootechnical feed additives for poultry. Approval would expand the portfolio of compliant mineral sources in the EU, requiring manufacturers to review formulation and sourcing strategies.

open.efsa.europa.euEuropean UnionEuropean Union

European Commission Adopts Implementing Regulation (EU) 2026/402 Authorising L-Cystine Produced With Escherichia coli DSM 34232 as a Feed Additive for All Animal Species

The EU has authorised L-cystine produced via E. coli DSM 34232 as a sensory feed additive for all animal species, effective March 17, 2026. Businesses must adhere to specific purity thresholds and labeling requirements for premixtures to maintain compliant market access through 2036.

eur-lex.europa.euEuropean UnionEuropean Union

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These are just a few of the most recent Amino Acids alerts. Foresight tracks every jurisdiction, every day — and surfaces only what affects your portfolio, with full citations and evidence.

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