Jan 16, 2023
Canada
The new article highlights the aspects related to situations when clinical data is not needed, as well as to the changes to medical devices and amendments to the respective applications. Table of Contents Health Canada, a country’s regulating authority in the sphere...
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Jan 16, 2023
EU MDR/IVDR
The article provides an overview of the guidance document explaining how Article 97 MDR should be applied to legacy devices. Table of Contents The Medical Device Coordination Group (MDCG), an advisory body of the European Commission in the sphere of medical devices,...
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Dec 7, 2022
Canada
The new article describes in detail the aspects related to the submission of clinical evidence in the context of applications for marketing approval. Table of Contents Health Canada, a country’s regulatory agency in the sphere of healthcare products, has published a...
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Dec 6, 2022
Canada
The article provides an overview of the regulatory requirement related to clinical evidence for medical devices. Table of Contents Health Canada, the country’s regulating authority in the sphere of healthcare products, has published a guidance document dedicated to...
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Nov 23, 2022
EU MDR/IVDR
The new article highlights the key points related to a change of authorized representative, as well as the ones related to responsible persons and marketing surveillance. Table of Contents The Medical Device Coordination Group (MDCG), an advisory body of the European...
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