CEOFOODLAW advises global food and beverage companies on anticipating, interpreting and complying with the Latin American regulatory environment — from the Codex Alimentarius to each country's health authority.
CEOFOODLAW works with a deliberately limited number of clients: international companies for which Latin America is a strategic market and regulation a business variable.
Additives, flavours, sweeteners and nutrition solutions requiring country-by-country admissibility.
Finished-product portfolios exposed to front-of-pack labelling, allergens and the ultra-processed agenda.
Companies entering Latin America — or expanding from it to other continents — that need to cross the regulatory barrier without surprises.
Every regulatory statement cites its official source — regulation, resolution, Codex session report or legislative bulletin — with dates. Where something is the firm's interpretation, it is declared as such.
The firm uses advanced artificial intelligence to monitor, process and analyse the regulatory environment at a speed no manual team can match. And one rule without exceptions: no deliverable reaches a client without validation by a regulatory expert. Technology provides the speed; expert judgement, the answer. Each client's information is handled under strict confidentiality protocols.
CEOFOODLAW operates with a network of associated consultants across Latin America's main markets — local specialists who know their health authority, their normative language and their real-world practice. Capacity on the ground, central coordination, one standard of quality.
Services built on one principle: every regulatory statement with its official source cited, every recommendation oriented to a business decision.
Continuous monitoring of authorities, parliaments and Codex across the markets that matter to your portfolio, with interpreted alerts — not newsletters.
Review and adaptation of labels to the detail of each jurisdiction: warning seals, allergens, claims, language and local requirements.
Assessment of whether an ingredient, additive or processing aid can be used in a market, under which limits and with what support.
Design of regulatory entry into one or several countries: sequencing, sanitary registration, technical dossier and coordination with the authority.
Expert interlocution before health authorities and participation in the forums where the rules are written.
Results of the 2026 Regional Consultation, distributed through five international sector organisations.
Receive on publicationA reading from inside the delegation: the adopted text and the likely national adoption timeline.
Read analysisWhere each bill stands, which definitions compete, and what it means for the most exposed categories.
Read analysisIf your organisation faces a decision with a regulatory component in Latin America, the first step is a direct conversation.
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