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Items: 16

1.

The European Union Directive on Clinical Research: present status of implementation in EU member states' legislations with regard to the incompetent patient.

Lemaire F, Bion J, Blanco J, Damas P, Druml C, Falke K, Kesecioglu J, Larsson A, Mancebo J, Matamis D, Pesenti A, Pimentel J, Ranieri M; ESICM Task Force on Legislation Affecting Clinical Research in the Critically Ill Patient.

Intensive Care Med. 2005 Mar;31(3):476-9. Epub 2005 Feb 15. No abstract available.

PMID:
15711974
2.

Informed consent for and regulation of critical care research.

Lemaire F.

Curr Opin Crit Care. 2008 Dec;14(6):696-9. doi: 10.1097/MCC.0b013e328315a62. Review.

PMID:
19005312
3.

[Simplification of procedures for clinical drug trials in the EU is coming up].

Bach KF, Jørgensen A.

Ugeskr Laeger. 2013 Nov 11;175(46):2778-81. Review. Danish.

PMID:
24629314
4.

The European Working Time Directive: effect on education and clinical care.

Waurick R, Weber T, Bröking K, Van Aken H.

Curr Opin Anaesthesiol. 2007 Dec;20(6):576-9. Review.

PMID:
17989553
5.

Capacity to consent to research in schizophrenia: the expanding evidence base.

Dunn LB.

Behav Sci Law. 2006;24(4):431-45. Review.

PMID:
16883608
6.

[Establishing ophthalmology in the research framework programs of the European Union].

Scholl HP, Wheeler-Schilling TH, Zrenner E, Holz FG.

Ophthalmologe. 2006 Feb;103(2):91-9. Review. German.

PMID:
16437232
7.

Legal requirements for the quality of herbal substances and herbal preparations for the manufacturing of herbal medicinal products in the European union.

Vlietinck A, Pieters L, Apers S.

Planta Med. 2009 Jun;75(7):683-8. doi: 10.1055/s-0029-1185307. Epub 2009 Feb 9. Review.

PMID:
19204891
8.

Biotechnology patenting policy in the European Union--as exemplified by the development in Germany.

Schrell A, Bauser H, Brunner H.

Adv Biochem Eng Biotechnol. 2007;107:13-39. Review.

PMID:
17522818
9.

Accurate dosimetry: an essential step towards good clinical practice in nuclear medicine.

Bacher K, Thierens HM.

Nucl Med Commun. 2005 Jul;26(7):581-6. Review.

PMID:
15942477
10.

[Blood transfusion in the European Union: current status and future challenges].

Rouger P.

Bull Acad Natl Med. 2006 Jan;190(1):189-203; discussion 203-4. Review. French.

PMID:
16878454
11.

The European Union Blood Safety Directive and its implications for blood services.

Robinson EA.

Vox Sang. 2007 Aug;93(2):122-30. Review.

PMID:
17683355
12.

The conduct of clinical trials for medicinal products in europe in the light of the European clinical trials directive. Review of regulatory and practical aspects in the different countries.

Dubray C, Maillere P, Spriet A; Round Table No 1, Giens XXII.

Therapie. 2007 May-Jun;62(3):193-7, 199-202. Epub 2007 Sep 6. Review. English, French.

13.

Towards eradication of bovine tuberculosis in the European Union.

Reviriego Gordejo FJ, Vermeersch JP.

Vet Microbiol. 2006 Feb 25;112(2-4):101-9. Epub 2006 Jan 4. Review.

PMID:
16388921
14.

[Present status of and tasks in guardianship for the mentally incompetent aged].

Saito M.

Seishin Shinkeigaku Zasshi. 2004;106(1):78-83. Review. Japanese. No abstract available.

PMID:
15154426
15.

Research in the European Union.

Sautter J, Wick R, Adlkofer F, Baker MG.

Lancet Neurol. 2003 Nov;2(11):702-6. Review. No abstract available.

PMID:
14572739
16.

Harmonizing standards and coding for hESC research.

Lomax G, McNab A.

Cell Stem Cell. 2008 Mar 6;2(3):201-2. doi: 10.1016/j.stem.2008.02.002. Review. No abstract available.

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