This chart illustrates the steps in the Australia TGA medical device approval process and includes a timeline of expected approval.
This chart illustrates the steps in the Brazil ANVISA medical device approval process and includes a timeline of expected approval.
Medical device manufacturers who want to enter the Costa Rican market need to obtain approval from the Costa Rican Ministry of Health. There are a few pathways to approval, and documentation requirements are different depending on your device's class.
这份白皮书介绍了MDR针对PMS和PSUR义务的新要求以及在全球QMS中实施这些要求所产生的风险。
此流程图阐明了英国每个医疗器械分类MHRA注册认证审批流程,可在法规事务管理平台(RAMS)下载。
This chart illustrates steps to CE Marking in Europe's Medical Devices Regulation (MDR 2017/745) approval process.
这份简短的检查清单将帮助您确定如何让您的体外诊断医疗器械公司符合欧盟IVDR。
此流程图阐明了沙特阿拉伯每个医疗器械分类的注册和SFDA认证审批流程,可在法规事务管理平台(RAMS)下载。