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Biostimulant legislation in Uruguay
Here, you can find the basic information about the legislation governing Biostimulants in Uruguay.
If you have any questions, reach out us.
Summary
The regulation of plant biostimulants (“_bioestimulantes vegetales_”) in Uruguay is still developing and recently the _Plan Nacional de Bioinsumos_was officially approved on February 20, 2025, by Decree n°042/025. In the meantime, there is a concrete regulatory framework you must follow.
The responsible competent authority in Uruguay for these matters is the [Ministerio de Ganadería, Agricultura y Pesca (MGAP), specifically its Dirección General de Servicios Agrícolas (DGSA)]. There is also a _Commission on Bioinsumos (COMBIO)_ within MGAP to coordinate regulatory work.
According to MGAP, “_bioinsumos_” include a variety of categories: plant protection (botanicals, semio-chemicals, biological control), as well as organic inputs (“ _insumos orgánicos formulados_”). Plant biostimulants fall under the latter. Specifically, biostimulants made from organic material (“_bioestimulantes de origen orgánico_”) are regulated under MGAP. The technical requirements for registering organic biostimulants are laid out in [Resolución DGSA No. 270/022 (Resolución 270/022). ] The resolution specifies required data, physical / chemical / sanitary specifications, categorization (humic substances, amino acids, algae extracts, plant extracts), and labelling requirements.
Given that the national bio-input plan is quite new (2025), there may be evolving policy or changes; it's wise to engage with MGAP early (e.g., via its DGSA) to understand the latest guidance.
Based on available public information, to place a biostimulant on the Uruguayan market you need to:
- Prepare a registration dossier following the technical requirements in _Resolución 270/022_mentioned above. This dossier will include data and information about product composition, physics-chemical properties, physical and biological properties, efficacy data or other justification of the claimed effects, a draft label.
- This dossier is to be submitted with the request for registration to the DGSA / MGAP, using the forms referenced in the Resolution 270/022.
- Pay the registration fee (15,000 U.I.). (this is around €325)
- make sure you will be able to comply with potential required post-registration obligations (if any). For example, for microbial control agents or other _bioinsumos_, there may be follow-up or reporting. (Note: check with DGSA for any post-market monitoring obligations.)
- For imported products: there may be additional import requirements (e.g., sanitary import permits) — check with MGAP and possibly the Uruguayan customs authority.
Do you need help with the registration process? Do you have any other question?
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The sciBASICS Team.
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