The European Directive 2001/20 for clinical research: friend or foe?
Author:
Publisher
Springer Science and Business Media LLC
Subject
Critical Care and Intensive Care Medicine
Link
http://link.springer.com/content/pdf/10.1007/s00134-006-0386-0.pdf
Reference12 articles.
1. Veelo D, Spronk P, Kuiper M, Korevaar J, van der Voort P, Schultz M (2006) A change in the Dutch Directive on medical research involving human subjects strongly increases the number of eligible intensive care patients: an observational study. Intensive Care Med DOI 10.1007/s00134-006-0384-2
2. van Dijk Y, van der Voort P, Kuiper M, Kesecioglu J (2003) Research on subjects incapable of giving consent: the situation in Dutch intensive care departments. Intensive Care Med 20:2100–2101
3. Harvey SE, Elbourne D, Ashcroft J, Jones C, Rowan K (2006) Informed consent in clinical trials in crtitical care: experience from the PAC-man study. Intensive Care Med
4. van der Voort P, Kesecioglu J (2006) Changes in the Dutch law on medical research. Intensive Care Med DOI 10.1007/s00134-006-0385-1
5. Meunier F, Lacombe C (2003) European organisation for research and treatment of cancer's point of view. Lancet 362:663
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