Clinical trials in an emergency setting: implications from the fifth version of the Declaration of Helsinki

Author:

Vanpee Dominique,Gillet J.B,Dupuis Michel

Publisher

Elsevier BV

Subject

Emergency Medicine

Reference11 articles.

1. Do patients with acute medical conditions have the capacity to give informed consent for emergency medicine research?;Smithline;Acad Emerg Med,1999

2. Efficacy and safety of thrombolytic therapy after initially unsuccessful cardiopulmonary resuscitation;Bottiger;Lancet,2001

3. Medical research in clinicalm emergency settings in Europe;Lotjonen;J Med Ethics,2002

4. Emergency medicine and the development of the Food and Drug Administration's final rule on informed consent and waiver of informed consent in emergency research circumstances;Biros;Acad Emerg Med,1998

5. European Parliament and the Council of the European Union. Directive 2001/20/EC of the European Parliament and the Council of 4 April 2001 on the approximation of the laws, regulations and administrative provisions of the Member States relating to the implementation of good clinical practice in the conduct of clinical trials on medicinal products for human use. Official Journal of the European Communities 2001 May 1. L 121/34

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