{"title":"利益相关者对瑞士医疗器械条例草案的看法","authors":"","doi":"10.54920/scto.2019.rawatch.2.12","DOIUrl":null,"url":null,"abstract":"To provide our readers with a good forecast of the changes ahead, the RA Watch editorial team asked different representatives – of the ethics committees umbrella organisation, the industry, and the SCTO network of CTUs – their views about the two ordinances proposed for consultation by the Federal Office of Public Health (FOPH). Their views and opinions refer to the drafted versions of the Medical Devices Ordinance (MedDO) and the ordinance on clinical trials for medical devices (ClinO-MD) as open to comments on 15 May 2019.","PeriodicalId":419230,"journal":{"name":"Regulatory Affairs Watch","volume":"47 2 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Stakeholders’ views on the Swiss draft ordinances on medical devices\",\"authors\":\"\",\"doi\":\"10.54920/scto.2019.rawatch.2.12\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"To provide our readers with a good forecast of the changes ahead, the RA Watch editorial team asked different representatives – of the ethics committees umbrella organisation, the industry, and the SCTO network of CTUs – their views about the two ordinances proposed for consultation by the Federal Office of Public Health (FOPH). Their views and opinions refer to the drafted versions of the Medical Devices Ordinance (MedDO) and the ordinance on clinical trials for medical devices (ClinO-MD) as open to comments on 15 May 2019.\",\"PeriodicalId\":419230,\"journal\":{\"name\":\"Regulatory Affairs Watch\",\"volume\":\"47 2 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Regulatory Affairs Watch\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.54920/scto.2019.rawatch.2.12\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Regulatory Affairs Watch","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.54920/scto.2019.rawatch.2.12","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Stakeholders’ views on the Swiss draft ordinances on medical devices
To provide our readers with a good forecast of the changes ahead, the RA Watch editorial team asked different representatives – of the ethics committees umbrella organisation, the industry, and the SCTO network of CTUs – their views about the two ordinances proposed for consultation by the Federal Office of Public Health (FOPH). Their views and opinions refer to the drafted versions of the Medical Devices Ordinance (MedDO) and the ordinance on clinical trials for medical devices (ClinO-MD) as open to comments on 15 May 2019.
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