* Strategic and market intelligence studies, articulation of partnerships to enable business, costs survey, deadlines, and documentation;
* Technical opinion for classification and assessment of regulatory feasibility of products and formulations;
* Licenses and company registration with ANVISA and MAPA;
* Registration and notification of products with ANVISA, MAPA and ANM;
* Inclusion and extension of the use of additives and technology adjuvants in the positive list;
* Inclusion of new ingredients and claims in supplements;
* Risk and effectiveness assessment for approval of new ingredients, new foods, and functional and/or health claims;
* Dossier for approval of “Genetically Modified Organisms” (GMO);
* “Good Practices Manual” and SOPs;
* Technical and scientific texts;
* Preparation or review of labeling and nutritional information;
* Nutritional marketing and communication: differentiation and enhancement of product characteristics, from labeling to the review and assembly of technical and promotional materials;
* Audits to comply with good regulatory practices and post-registration management of companies and products;
* Comprehensive Technical Support and Audits (Due Diligence);
* Support and preparation of technical defenses with legal support in support of product and company inspection: notice of infraction and seizure, interdiction, notifications, letters, and fines.