All In vitro diagnostic devices articles
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Industry newsEC announces evaluation of medical device and IVD regulations
The European Commission (EC) has announced an evaluation of Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnostic medical devices.
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JournalMD2/IVD2:
Medical technologies −
a catalyst for
regulatory innovationsRegulatory Rapporteur December 2023 | Volume 20 | No.11 Session leader Alwin van den Broek, Medical Devices Professional, the Netherlands. Maaike Labots, Manager Medical Writing, Avania Clinical, the Netherlands. Speakers and panelists Maryam Atakhorrami, Global ...
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JournalIVD5: Class D IVDs
Regulatory Rapporteur December 2023 | Volume 20 | No.11 Session Leader Amanda Brown, Director of Quality and Regulatory Affairs, HP, Germany. Ashleigh Batchen, Regulatory Strategy Principal (UK), TÜV SÜD, UK. Speakers and panelists Olga Tkachenko, ...
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JournalIVD3: IVDR: Current state
Regulatory Rapporteur December 2023 | Volume 20 | No.11 Session leads: Amanda Brown, Director of Quality and Regulatory, HP, Germany. Ashleigh Batchen, Regulatory Strategy Principal, TÜV SÜD, UK. Speakers: Olga Tkachenko, Scientific Policy Officer, European ...
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