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CTD MODULO 3
Lisboa, 26 de fevereiro de 2025
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Recentes
510(k) Third Party Review Program and Third Party Emergency Use Authorization (EUA) Review
Marketing Submission Recommendations for a Predetermined Change Control Plan for Artificial Intelligence-Enabled Device Software Functions
Total Product Lifecycle Considerations for Generative AIEnabled Devices
MDCG 2024-15 – Guidance on the publication of the clinical investigation reports and their summaries in the absence of EUDAMED (November 2024)
Team-NB High level position on the regulatory framework for the medical devices sector
CONTROLO DE ALTERAÇÕES : Sessão esclarecedora com uma discussão bastante interessante sobre o assunto
EU Prosperity and Competitiveness: Recommendations for implementing the EU Green Deal in Healthcare
Consultation on ICH E6 (R3) Guideline for Good Clinical Practice Annex-2