[Not Available].
作者信息
Hildebrand Heidrun
机构信息
Bayer AG, Pediatric Development.
出版信息
Drug Res (Stuttg). 2018 Nov;68(S 01):S16-S17. doi: 10.1055/a-0731-7667. Epub 2018 Nov 19.
PMID:30453368
Abstract
摘要
相似文献
1
[Not Available].[无可用内容]
Drug Res (Stuttg). 2018 Nov;68(S 01):S16-S17. doi: 10.1055/a-0731-7667. Epub 2018 Nov 19.
2
Clinical trials: consent in children.
Expert Rev Vaccines. 2005 Feb;4(1):1-3. doi: 10.1586/14760584.4.1.1.
3
New European regulation for clinical trials of medicinal products.
Am J Respir Crit Care Med. 2015 Jan 1;191(1):16-8. doi: 10.1164/rccm.201406-1038ED.
4
Elements of informed consent.知情同意的要素
MCN Am J Matern Child Nurs. 1996 Jul-Aug;21(4):205. doi: 10.1097/00005721-199607000-00027.
5
Evaluation of treatments is threatened by EC directive.
BMJ. 2002 Jul 27;325(7357):222.
6
Provision of consent.提供同意书。
Lancet. 2003 Aug 23;362(9384):664. doi: 10.1016/S0140-6736(03)14165-7.
7
Clinical trials. How informed should consent be?临床试验。知情同意应达到何种程度？
RN. 2000 Jun;63(6):77-82.
8
[Harmonisation of regulatory requirements for clinical trials on medicinal products for human use in the Directive 2001/20/EC and complementary guidance. Implementation of the 12th Law Amending the German Drug Law].[协调2001/20/EC指令中关于人用药品临床试验的监管要求及补充指南。德国药品法第12次修订案的实施]
Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2005 Feb;48(2):141-6. doi: 10.1007/s00103-004-0978-1.
9
[Not Available].[无可用内容]。
Drug Res (Stuttg). 2018 Nov;68(S 01):S2. doi: 10.1055/a-0731-6178. Epub 2018 Nov 19.
10
Deficiencies in proposed new EU regulation of clinical trials.欧盟新提议的临床试验法规存在的缺陷。
BMJ. 2012 Dec 20;345:e8522. doi: 10.1136/bmj.e8522.
Zotero 插件