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1
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EU |
(EU)Guidlines on the Quilification and Classification of Stand Alone Software Used in Healthcare within the Regulatory Framework of Medical Deivces, 2020
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2
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EU |
(EU)General leaflet ATI Policy Brief reports, 2021
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3
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EU |
(EU)Advanced technology landscape and related policies in China, 2021
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4
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(EU)proposal-for-a-regulation-laying-down-harmonised-rules-on-artificial-intelligence-impact-on-the-healthcare-sector-and-the-medical-device-industry, 2021
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5
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EU |
(EU)Advanced Technologies for Industry – Product Watch_Artificial Intelligence-based software as a medical device, 2020
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6
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EU |
(EU)Guidance on Qualification and Classification of Software in Regulation, 2019
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7
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EU |
(EU)Guidance on significant changes regarding the transitional provision under Article 120 of the MDR with regard to devices covered by certificates according to MDD or AIMDD, 2016
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8
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EU |
“MDCG 2020-3: Guidance on significant changes regarding the transitional provision under Article 120 of the MDR with regard to devices covered by certificates according to MDD or AIMDD”, 2020.
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9
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EU |
“MDCG 2019-11:Guidance on Qualification and Classification of Software in Regulation (EU) 2017/745-MDR and Regulation (EU) 2017/746-IVDR”, 2019.
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10
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EU |
“REGULATION (EU) 2017/745 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL, 2017.
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