Reports on the plans to upgrade the European Union regulations governing dietary supplements and herbal products. Opposition of consumers to restrictions set on dietary supplements; Overview of the outdated re...
Medical Devices – New regulations
a consultation on proposed legislation, The Medicines for Human Use (Clinical Trials) Regulations, to implement the European Union Clinical Trials Directive. ... Corrigan,Oonagh,P,... - 《Lancet》 被引量: 42发表: 2003年 European Medicines Agency Evaluation of Medicines for Human Use a consultati...
Proposalfor a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards the transitional provisions for certain medical devices and in vitro diagnostic medical devices. Fact sheet:Supporting the transition to the new medical device fra...
Medical Devices – New regulations Source: European Commission
REGULATION (EU) 2017/746 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU 文档格式: .pdf 文档大小: 2.01M 文档页数: ...
https://ec.europa.eu/health/md_sector/new_regulations/guidance_en MDCG 所有模块下医疗器械的相关指南文件 EUDAMED数据库 https://ec.europa.eu/health/md_eudamed/actors_registration_en 欧盟EUDAMED数据库 Team NB https://www.team-nb.org/
Proposed reforms to the regulations for PBMs were dropped from the US Congress' end-of-year bill to provide funding to the federal government. Digital Sponsored The AI effect in pharma commercial strategy: From data to re... Discover how AI is transforming the pharma commercial strategy. Unl...
medical device in humans.The law considering MDs in European Community is composed of 2 regulations:2017/745/EC(medical devices)and 2017/746/EC(in vitro... Jan,W Borowiec 被引量: 0发表: 2017年 Comments on the EU White Paper on AI: A Regulatory Framework for High-Risk Healthcare AI Appl...
(IMDRF), should be taken into account to promote the global convergence of regulations which contributes to a high level of safety protection worldwide, and to facilitate trade, in particular in the provisions on Unique Device Identification, general safety and performance requirements, technical ...