Commentary: Europe needs a central, transparent, and evidence based regulation process for devices

被引：30

作者：

Eikermann, Michaela ^{[1
]}

Gluud, Christian ^{[2
]}

Perleth, Matthias ^{[3
]}

Wild, Claudia ^{[4
]}

Sauerland, Stefan ^{[5
]}

Gutierrez-Ibarluzea, Inaki ^{[6
]}

Antoine, Sunya-Lee ^{[1
]}

Demotes-Mainard, Jacques ^{[7
]}

Neugebauer, Edmund A. M. ^{[1
]}

机构：

[1] Univ Witten Herdecke, Sch Med, Fac Hlth, Inst Res Operat Med, D-51109 Cologne, Germany

[2] Copenhagen Univ Hosp, Ctr Clin Intervent Res, Copenhagen Trial Unit, Copenhagen, Denmark

[3] German Soc Technol Assessment Hlth Care, Berlin, Germany

[4] Ludwig Boltzmann Inst Hlth Technol Assessment, Vienna, Austria

[5] Inst Qual & Efficiency Healthcare IQWiG, Cologne, Germany

[6] Osteba, Basque Off Hlth Technol Assessment, Vitoria, Spain

[7] INSERM, Inst Themat Sante Publ, Paris, France

来源：

BMJ-BRITISH MEDICAL JOURNAL | 2013年 / 346卷

基金：

英国医学研究理事会;

关键词：

D O I：

10.1136/bmj.f2771

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页数：2