Will a NB designated under MDR/IVDR will be able to assess the conformity of a MD incorporating AI?Will a NB designated under MDR/IVDR will be able to assess the conformity of a MD incorporating AI?Team NB (European Association of Medical devices Notified Bodies) has...
Publications : Matières premières
COCIR Artificial Intelligence in EU Medical Device Legislation
COCIR Artificial Intelligence in EU Medical Device LegislationCOCIR Artificial Intelligence in EU Medical Device LegislationCOCIR published an analysis in 2020 on AI-based devices in the scope of MDR and IVDR. The purpose of this analysis is to provide an update on...
GDPR
GDPRGDPRThe GDPR (General Data Protection Regulation 2016/679) sets limits on the use of personal data considered sensitive. It provides many opportunities for effective monitoring and enforcement of fairness, transparency, individual rights and granting individual...
Public Health Code – Bioethics law
Public Health Code - Bioethics lawPublic Health Code - Bioethics lawThe bioethics law after several revisions was finally adopted in August 2021. In its draft format, Article 11 of this law, which became Article 17 in its final format, introduces a legal framework for...
Proposal for a directive of the European parliament and of the council on adapting non-contractual civil liability rules to articial intelligence (AI liability Directive)
Proposal for a directive of the European parliament and of the council on adapting non-contractual civil liability rules to articial intelligence (AI liability Directive)Proposal for a directive of the European parliament and of the council on adapting non-contractual...
New rules for Artificial Intelligence – Questions and Answers
New rules for Artificial Intelligence – Questions and AnswersNew rules for Artificial IntelligenceThe new rules for artificial intelligence are a set of guidelines developed by the European Commission to regulate the use of artificial intelligence (AI) in the European...
Proposed Regulation on Artificial Intelligence
Proposed Regulation on Artificial IntelligenceArtificial Intelligence RegulationThe publication in April 2021 of the European Commission’s proposal for a European regulation on artificial intelligence is part of a global desire by all stakeholders to define the...
MDCG 2022-20 Substantial modification of performance study under Regulation (EU) 2017/746 – December 2022
Theme Substantial modification of performance study Target Audience Sponsors, Competent authorities Products concerned IVD Regulatory reference IVDR (EU) 2017/746 Article 66(1) Article 70(1) Article 71 Documents mentioned MDCG 2022-19 As the EUDAMED database is...
MDCG 2022-19 Performance study application/notification documents under Regulation (EU) 2017/746 – December 2022
Theme Application/notification for performance studies Target Audience Sponsors, Competent authorities Products concerned IVD Regulatory reference IVDR (EU) 2017/746 Article 66 Article 69 Article 70(1) Documents mentioned MDCG 2022-12 As the EUDAMED database is...
MDCG 2022-18 : MDCG Position Paper on the application of Article 97 MDR to legacy devices for which the MDD or AIMDD certificate expires before the issuance of a MDR certificate – December 2022
Theme Legacy devices Target Audience Manufacturers, Notified bodies Products concerned MD Regulatory reference MDR (EU) 2017/745 Documents mentioned MDCG 2020-3 MDCG 2021-25 This position paper concerns legacy medical devices, i.e. devices with an MDD or AIMDD...