Medical device annual reporting – Sponsor obligations
Medical Device Expert News
Use of Symbols to Indicate Compliance with the MDR
Programação da X Jornada de Ação em Política Industrial e Regulação para Produtos da Saúde
MDCG 2018-1 v2 Guidance on basic UDI-DI and changes to UDI-DI
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ANVISA – INSTRUÇÃO NORMATIVA N° 32, DE 12 DE ABRIL DE 2019
Guidance Document: Supporting Evidence for Implantable Medical Devices Manufactured by 3D Printing
Webinar: An update on the consultation for the Regulation of Software, including Software as a Medical Device (SaMD)
Guidance on the Systematic Review process in ISO Guidance on new work My ISO job – What delegates and experts need to know How to…
A ISO 13485:2016 se encontra em processo de análise crítica sistemática (para maiores informações sobre o processo, favor acessar o guia Guidance on the Systematic…