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MedTech published recommendations on the use of guidance documents,
in Uncategorized
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Obligations for authorised representatives, importers and distributors,
in Uncategorized
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MDCG published a Q&A on the interface between Regulation (EU) 536/2014 on clinical trials for medicinal products for human use (CTR) and Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR),
in Uncategorized
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Commission publishes information on the status of the EU-Switzerland Mutual Recognition Agreement (MRA) for in vitro diagnostic medical devices,
in Uncategorized
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3 New MDCG documents published,
in Uncategorized
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MDCG 2022-6 published on Guidance on significant changes regarding the transitional provision under Article 110(3) of the IVDR,
in Uncategorized
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Updated MDCG Joint Implementation Plan on IVDR,
in Uncategorized
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MDCG publishes revision 1 of 2019-9 about SSCP,
in Uncategorized
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MDCG 2022-4 published: Notified Body surveillance of MDR legacy devices,
in Uncategorized
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Publication in Official Journal of the European Union about the transitional periods of the IVDR,
in Uncategorized
