All documents listed below were published by Saudi Food and Drug Authority (SFDA) and are in PDF format.
Based on the Council of Ministers resolution no. (181) issued on 18/6/2007, that gave SFDA the right to issue regulations for medical devices registration rules and procedures, the SFDA issued a medical devices interim regulation, which was adopted by SFDA board of director’s decision no. (1-8-1429) issued on 27/12/2008. This regulation will apply until the medical devices comprehensive law is approved.
自2018年起,美国食品和药物管理局(U.S. Food and Drug Administration,FDA)开始试行以电子化方式来帮助行业提供完整的510(k)上市前通知。2022年,为推进以电子格式提供510(k)递交文件的过渡,美国FDA正式发布关于使用电子递交模板和资源的最终指导文
阅读更多新欧盟医疗器械法规2017/745(MDR)新增了对公告机构开展临床评估审查的新要求。该审查新要求的提出将对部分在从医疗器械法令MDD到新医疗器械法规MDR过渡中的医疗器械企业带来面临不符合项的风险。 对此,此场研讨会将特此分享在新欧盟医疗器械法规MDR下,医疗器械如何满足临床评
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