Artigos recentes

• EMA new guidelines on veterinary pharmacovigilance
• Veterinary product information templates
• MDCG 2021-19 Guidance note integration of the UDI within an organisation’s quality management system
• The FDA finalized its guidance on the form and content requirements for unique device identifiers (UDI)
• 4th Edition of the ISO 15223-1:2021 Medical devices — Symbols to be used with information to be supplied by the manufacturer — Part 1: General requirements
• Fichas informativas com informação básica para todos os stakeholders sobre os novos Regulamentos dos Dispositivos Médicos e Dispositivos Médicos para o diagnóstico in vitro
• EXPAMED CECP (Opinion in the context of Cllinical Evaluation Consultation Procedure).
• EMA has published version 2.1 of the Implementation Guide for the ISO IDMP standards