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Tarricone, Rosanna 
ORCID: https://orcid.org/0000-0002-2009-9357; Banks, Helen ORCID: https://orcid.org/0000-0003-0337-1715; Ciani, Oriana ORCID: https://orcid.org/0000-0002-3607-0508; Brouwer, Werner ORCID: https://orcid.org/0000-0002-0476-8397; Drummond, Michael F ORCID: https://orcid.org/0000-0002-6968-4610; Leidl, Reiner ORCID: https://orcid.org/0000-0002-7115-7510; Martelli, Nicolas ORCID: https://orcid.org/0000-0001-5959-231X; Sampietro-Colom, Laura ORCID: https://orcid.org/0000-0001-7182-0231 und Taylor, Rod S. ORCID: https://orcid.org/0000-0002-3043-6011
(3. April 2023):
An accelerated access pathway for innovative high-risk medical devices under the new European Union Medical Devices and health technology assessment regulations? Analysis and recommendations.
In: Expert Review of Medical Devices, Bd. 20, Nr. 4: S. 259-271
[PDF, 2MB]
ORCID: https://orcid.org/0000-0002-2009-9357; Banks, Helen ORCID: https://orcid.org/0000-0003-0337-1715; Ciani, Oriana ORCID: https://orcid.org/0000-0002-3607-0508; Brouwer, Werner ORCID: https://orcid.org/0000-0002-0476-8397; Drummond, Michael F ORCID: https://orcid.org/0000-0002-6968-4610; Leidl, Reiner ORCID: https://orcid.org/0000-0002-7115-7510; Martelli, Nicolas ORCID: https://orcid.org/0000-0001-5959-231X; Sampietro-Colom, Laura ORCID: https://orcid.org/0000-0001-7182-0231 und Taylor, Rod S. ORCID: https://orcid.org/0000-0002-3043-6011
(3. April 2023):
An accelerated access pathway for innovative high-risk medical devices under the new European Union Medical Devices and health technology assessment regulations? Analysis and recommendations.
In: Expert Review of Medical Devices, Bd. 20, Nr. 4: S. 259-271
[PDF, 2MB]
Tarricone, Rosanna ORCID: https://orcid.org/0000-0002-2009-9357; Ciani, Oriana ORCID: https://orcid.org/0000-0002-3607-0508; Torbica, Aleksandra ORCID: https://orcid.org/0000-0001-8938-7608; Brouwer, Werner ORCID: https://orcid.org/0000-0002-0476-8397; Chaloutsos, Georges; Drummond, Michael F ORCID: https://orcid.org/0000-0002-6968-4610; Martelli, Nicolas ORCID: https://orcid.org/0000-0001-5959-231X; Persson, Ulf; Leidl, Reiner ORCID: https://orcid.org/0000-0002-7115-7510; Levin, Les; Sampietro-Colom, Laura und Taylor, Rod S ORCID: https://orcid.org/0000-0002-3043-6011
(2020):
Lifecycle evidence requirements for high-risk implantable medical devices: a European perspective.
In: Expert Review of Medical Devices, Bd. 17, Nr. 10: S. 993-1006
[PDF, 2MB]
ORCID: https://orcid.org/0000-0002-2009-9357; Ciani, Oriana ORCID: https://orcid.org/0000-0002-3607-0508; Torbica, Aleksandra ORCID: https://orcid.org/0000-0001-8938-7608; Brouwer, Werner ORCID: https://orcid.org/0000-0002-0476-8397; Chaloutsos, Georges; Drummond, Michael F ORCID: https://orcid.org/0000-0002-6968-4610; Martelli, Nicolas ORCID: https://orcid.org/0000-0001-5959-231X; Persson, Ulf; Leidl, Reiner ORCID: https://orcid.org/0000-0002-7115-7510; Levin, Les; Sampietro-Colom, Laura und Taylor, Rod S ORCID: https://orcid.org/0000-0002-3043-6011
(2020):
Lifecycle evidence requirements for high-risk implantable medical devices: a European perspective.
In: Expert Review of Medical Devices, Bd. 17, Nr. 10: S. 993-1006
[PDF, 2MB]