Low-impact pesticides to control diseases and pests are new alternatives for farmers.
Published on December 7th, in the Diário Oficial da União [Federal Official Gazette], Act No. 57 of the Department of Plant Health and Agricultural Inputs of the Secretary for Agricultural Defense, presents the registration of 45 new agricultural pesticides formulated, which will …
Addition of new subjects of RDC 219/2018 must be filed by companies
Regarding the understanding of the rule that deals with the conditional approval of post-registration petitions for drugs (RDC 219/2018), Anvisa informs companies about its recent amendment. Subjects related to pharmaceutical technology and active substance of biological products were included According to the …
Digital medication package inserts begin to be regulated by Anvisa.
Nowadays, it is the Resolution 47 of Anvisa’s Board of Directors (RDC), from September 8, 2009, that establishes the rules for the development, standardization, updating, publication and provision of medication package inserts. However, this year, the Act no. 14,338 from 2022 was …
Understand the amendments to nutrition labeling rules.
On October 13, corrections were published that contribute to ensuring clarity, objectivity, and consistency of the Resolution of the Collegiate Board of Directors (RCBD) [Resolução da Diretoria Colegiada – RDC] 429/2020 and Normative Instruction 75/2020. In the meantime, the General Management of …
Anvisa publishes guidelines on microbiological control of cosmetics.
Last Monday, October 3, the Resolution of the Collegiate Board of Directors (RCBD) [Resolução da Diretoria Colegiada – RDC] 752/2022 came into force, which provides for the regularization of personal hygiene products, cosmetics, and perfumes. This is the first in a series …
Check the updated version of the Cadifa Manual of Administrative Procedures.
Anvisa has just published the third version of the Cadifa Manual on administrative procedures. The document was updated due to the migration of the petition of matters related to Cadifa (Adequacy Letter of Active Pharmaceutical Input Dossier) to the Solicita System, following …
Do I need a Company Operation Authorization (AFE, in Portuguese)?
If you own a company that operates in the health, cosmetics, sanitizing and pharmaceutical industries, the Company Operation Authorization (AFE) is one of the steps in your company’s regularization process. Among a series of norms and standards, it regulates safety in facilities, …
New FoodTech projects will be selected by public notice from September onwards.
The Ministry of Agriculture, Livestock, and Supply (MAPA) have published a public selection call for proposals focusing on contemporary food systems, new ingredients, alternative proteins, and new food technologies. Launched on August 22, the project is articulated with the National Fund for …
The transition process of Inmetro’s regulatory model gains new guidelines.
On August 3, Ordinance No. 286, of July 27, 2022, was signed, approving the governance process and instituting the transition committee for Inmetro’s regulatory model. Alexandre Ywata, Special Secretary for Productivity and Competitiveness (Sepec), was visiting the Dr. Arménio Lobo da Cunha …
Solicita System receives migration of new subjects.
From now on, notifications of temporary and permanent discontinuation of manufacturing and reactivation of medicines manufacturing can be found in the Solicita System. Due to this migration, current requests should only be made electronically. Despite the change, the codes for electronic petitioning …