Medicinal products with a medical device component (combination products) – Implementation of the transitional provisions for medical devices
16 juin 2023 – In the EU, an amendment was published to the EU-MDR on 20 March 2023 regarding the transitional period for medical device certificates issued under the old legislation (MDD). Swissmedic is following the European regulations on medical devices and is already implementing enforcement for medical devices according to the requirements of the revised EU-MDR in the transitional phase until the Swiss Medical Devices Ordinance (MedDO) is revised.
For more information, see here.