A CADIFA is a ANVISA letter that verifies the acceptance of the API dossier or Drug Master File (DMF), which includes basic API information.
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May 10, 2022 · A CADIFA is a letter from ANVISA showing that a DIFA, which is a certain DMF together with other administrative documents, was evaluated by them ...
Since then, Anvisa has issued the Letter of Suitability of the Active Pharmaceutical Ingredient (CADIFA) for APIs used in the manufacture of new, innovator ...
Oct 13, 2023 · A CADIFA is an ANVISA letter that verifies the acceptance of the API dossier or Drug Master File (DMF). It acts as a certificate of Good ...
Jun 22, 2023 · A CADIFA is a letter from Anvisa meaning that a certain drug master file (DMF) was evaluated by the agency and considered to be approved.
Feb 24, 2022 · The new version of the "CADIFA Manual for Administrative Procedures" of the Brazilian Health Regulatory Agency (Anvisa) was published in ...
The Carta de Adequabilidade do Dossiê de Insumo Farmacêutico Ativo (CADIFA) is a regulatory document or letter by the Agência Nacional de Vigilância Sanitária ( ...
The new regulatory framework for Active Pharmaceutical Ingredients (APIs/IFAs) of the Brazilian Health Regulatory Agency (ANVISA) comes into force. Foreign ...
1º This Resolution institutes the Active Pharmaceutial Ingredient Dossier (DIFA) and the Letter of. Suitability of the Active Pharmaceutical Ingredient (CADIFA) ...
Mar 12, 2024 · The application form template is structured for all types of applications. Additionally, Anvisa suggests the submission of the Comparative Table ...