Artigos recentes

• Publicada a nova versão da metodologia de avaliação farmacoterapêutica de tecnologias de saúde
• Big data use for public health: publication of Big Data Steering Group workplan 2022-25
• Global regulators call for international collaboration to integrate real-world evidence into regulatory decision-making
• FDA Evaluation of Therapeutic Equivalence Guidance for Industry
• EUROPEAN COMMISSION Serialization – Version 20 of the Q&As on Safety Features
• MedTech Europe Survey Report analysing the availability of In vitro Diagnostic Medical Devices (IVDs) in May 2022 when the new EU IVD Regulation applies
• NEW Industry contact points for supply and availability of critical medicines
• EMA launches pilot project on analysis of raw data from clinical trials