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Regulation (EU) 2025/327 of the European Parliament and of the Council of 11 February 2025 on the European Health Data Space and amending Directive 2011/24/EU and Regulation (EU) 2024/2847 (Text with EEA relevance)

article  34

CELEX:  32025R0327

Cases in which obligations of manufacturers of an EHR system apply to other entities or individuals An importer, distributor or user shall be considered a manufacturer for the purposes of this Regulation and shall be subject to the obligations laid down in Article 30 where they:
(a) make an EHR system available on the market under their own name or trademark;
(b) modify an EHR system already placed on the market in such a way that conformity with the applicable requirements might be affected; or (c) modify an EHR system in such a way that it leads to changes in the intended purpose declared by the manufacturer.