![New Recommendation to Swiss Medical Device Manufacturers](https://www.regdesk.co/wp-content/uploads/2019/12/swiss.jpg)
Jul 13, 2020
Europe
The SwissMedic, the authority responsible for medical device regulations in Switzerland, has published, in coordination with the EU and MDR, updated regulations: new Medical Devices Ordinance (MedDO) and Clinical Trials for Medical Devices Ordinance (ClinO-MD). These...
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![New Recommendation to Swiss Medical Device Manufacturers](https://www.regdesk.co/wp-content/uploads/2019/12/swiss.jpg)
Dec 18, 2019
Europe
Switzerland is going to amend its current medical device regulations in response to the changes implemented by Regulation 2017/745 (MDR). Mutual Recognition Agreement A mutual recognition agreement in the area of conformity assessment (MRA) is the most...
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![New Recommendation to Swiss Medical Device Manufacturers](https://www.regdesk.co/wp-content/uploads/2019/04/Switzerland-geo-flag.aspx_.jpeg)
Apr 30, 2019
Europe
Swiss Medtech Group, the non-governmental association that represents the interests of the companies operating within the medtech industry, issued recommendations to medical device manufacturers covering issues related to gaining access to various markets within the...
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