Order:
  1.  1
    Possible Health Technology Assessment Pathways.Mireia Espallargues Carreras, Xavier Garcia Cuscó, Rossana Alessandrello, Ramon Maspons, Alexandre Serigado, Cécile F. Rousseau, Emmanuelle M. Voisin, Enrique Morales-Orcajo & Marco Viceconti - 2024 - In Marco Viceconti & Luca Emili (eds.), Toward Good Simulation Practice: Best Practices for the Use of Computational Modelling and Simulation in the Regulatory Process of Biomedical Products. Springer Nature Switzerland. pp. 73-92.
    No categories
    Direct download  
     
    Export citation  
     
    Bookmark  
  2. Ethical Review of In Silico Methodologies.Cécile F. Rousseau, Emmanuelle M. Voisin, Elisabetta Poluzzi, Alexandre Serigado, Marco Viceconti & Maria Cristina Jori - 2024 - In Marco Viceconti & Luca Emili (eds.), Toward Good Simulation Practice: Best Practices for the Use of Computational Modelling and Simulation in the Regulatory Process of Biomedical Products. Springer Nature Switzerland. pp. 93-100.
    No categories
    Direct download  
     
    Export citation  
     
    Bookmark  
  3. Possible Qualification Pathways for In Silico Methodologies.Marco Viceconti, Alexandre Serigado, Cécile F. Rousseau & Emmanuelle M. Voisin - 2024 - In Marco Viceconti & Luca Emili (eds.), Toward Good Simulation Practice: Best Practices for the Use of Computational Modelling and Simulation in the Regulatory Process of Biomedical Products. Springer Nature Switzerland. pp. 67-72.
    Regulatory science is ultimately a matter of trust. You need to trust that certain evidence, when obtained with certain methodologies, is sufficient to inform about a new medical product's safety and/or efficacy.
    No categories
    Direct download  
     
    Export citation  
     
    Bookmark