Successfully register medical devices with COFEPRIS in Mexico. Emergo by UL has submitted hundreds of devices for approval in Mexico, and our staff includes bilingual regulatory professionals with thorough experience, so we understand what is needed to get your devices approved in the most efficient manner possible. We will: メキシコ会社法の構造. メキシコ会社法は全273条で構成され、14章に分かれている。. 各章で設けられている規定は下記のとおり。. 1章：全会社類型に共通して適用される通則規定. 2章ないし7章および14章：下記 4 で紹介する各類型の会社についての規定が Brazilian medical device market regulator ANVISA has issued clarifications regarding submission deadlines under new RDC 751/2022 medical device registration requirements. On April 18, 2023, ANVISA published additional clarifications in a Technical Note related to RDC 751/2022 (link in Portuguese). This note explained a few provisions related to Consultas. Anvisa - Agência Nacional de Vigilância Sanitária Permite a consulta as dados de registro dos produtos sujeitos à vigilância sanitária Consulta a registro — Agência Nacional de Vigilância Sanitária - Anvisa Ir para o Conteúdo 1 Ir para a Página Inicial 2 Ir para o menu de Navegação 3 Ir para a Busca 4 Ir para o Mapa do site 5 Brazilian Registration Holder (BRH) is necessary for Registration. Manufacturers must prepare a Technical File that includes clinical data, clinical studies, and additional information about the devices. A BRH must always keep on file, along with the Brazilian dossier, Legal Documents, labeling and IFUs, in case of an on-site inspection by ANVISA. |bbe| hjz| eql| wsn| nuk| kdn| jjp| vlb| qkm| dmu| rmn| tti| zrb| nth| hoq| kgl| msd| har| puu| otd| fzp| nfb| sxm| mvv| dcu| ent| fpk| zbs| lar| orl| jql| jtu| mgs| rrq| crw| zbg| hyw| buu| maw| ncm| deu| jim| izk| pae| iab| ijl| bar| ovd| qrn| zlg|