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...
Publications : Clinical trials
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...
MDCG 2022-17 : MDCG position paper on ‘hybrid audits’– December 2022
Theme Hybrid audits Target Audience Notified bodies, Manufacturers Products concerned MD/IVD Regulatory reference MDR (EU) 2017/745IVDR (EU) 2017/746 Documents mentioned MDCG 2020-4 MDCG 2020-17 MDCG 2022-14 This MDCG document clarifies the definitions and...
Yani Ammar
From a training focused on the creation of medical devices and the challenges around its design in terms of biomechanics and biocompatibilities. I pursued the construction of my knowledge at the international level by carrying out an R&D project for class III...
Laurence Corral
My career path has allowed me to explore different visions of the medical device field: the vision of the industry, mainly as Regulatory Affairs Manager, and then that of the notified body as Technical Documentation Evaluator. These different experiences have forged...
Marian Kunde
Following a beginning of study in physics and engineering science where I did not see the end. I became a self-taught photographer, which led me to try to share as much as possible the art I was producing. So I learned about techniques to catch the eye of the crowd,...
Switzerland – non-renewal of the Mutual Recognition Agreement with the EU: adjustments or real upheaval?
Switzerland non-renewal of the Mutual Recognition Agreement with the EU: adjustments or real upheaval?Switzerland - non-renewal of the Mutual Recognition Agreement with the EU: adjustments or real upheaval?Since 2002, a Mutual Recognition Agreement (MRA) has linked...