Anvisa updates rules for RDC nº 185/2001 - regulation of medical devices in Brazil Anvisa released on its website on Wednesday (14/09) a news informing about the update of the rules for regularization of medical devices in Brazil. According to Anvisa, the Collegiate Board approved the proposal that revises RDC 185/2001, [...]
Anvisa now requires digital signatures in medical device processes and petitions The National Health Surveillance Agency – ANVISA circulated this week through Solicita System the Circular Letter No. 1/2022/SEI/GGTPS/DIRE3/ANVISA, which mainly provides with guidelines for signatures in process and petition documents for medical devices. In this letter, Anvisa informs that [...]
PASSARINI GROUP is pleased to inform that PASSROD, one of the group's companies, has joined ABIMED Associação Brasileira da Indústria de Tecnologia para Saúde, entidade que aproxima indústria e governo, colaborando com a construção de políticas públicas voltadas ao setor, sendo também protagonista na criação de um ambiente favorável à [...]
