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3. Informed consent document improvement does not increase patients' comprehension in biomedical research. Paris A; Brandt C; Cornu C; Maison P; Thalamas C; Cracowski JL Br J Clin Pharmacol; 2010 Mar; 69(3):231-7. PubMed ID: 20233193 [TBL] [Abstract][Full Text] [Related]
4. French adaptation and preliminary validation of a questionnaire to evaluate understanding of informed consent documents in phase I biomedical research. Paris A; Cornu C; Auquier P; Maison P; Radauceanu A; Brandt C; Salvat-Melis M; Hommel M; Cracowski JL Fundam Clin Pharmacol; 2006 Feb; 20(1):97-104. PubMed ID: 16448400 [TBL] [Abstract][Full Text] [Related]
5. Readability of pediatric biomedical research informed consent forms. Tarnowski KJ; Allen DM; Mayhall C; Kelly PA Pediatrics; 1990 Jan; 85(1):58-62. PubMed ID: 2296494 [TBL] [Abstract][Full Text] [Related]
6. Determination of required content of the informed consent process for human participants in biomedical research conducted in the U.S. A practical tool to assist clinical investigators. Chanaud CM Contemp Clin Trials; 2008 Jul; 29(4):501-6. PubMed ID: 18249042 [TBL] [Abstract][Full Text] [Related]
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9. Informed consent in clinical research at a general hospital in Mexico: opinions of the investigators. Vargas-Parada L; Kawa S; Salazar A; Mazön JJ; Flisser A Dev World Bioeth; 2006 Mar; 6(1):41-51. PubMed ID: 16436173 [TBL] [Abstract][Full Text] [Related]
10. [Informed consent in clinical practice and medical research]. Santillan-Doherty P; Cabral-Castañeda A; Soto-Ramírez L Rev Invest Clin; 2003; 55(3):322-38. PubMed ID: 14515678 [TBL] [Abstract][Full Text] [Related]
11. Informed consent for and regulation of critical care research. Lemaire F Curr Opin Crit Care; 2008 Dec; 14(6):696-9. PubMed ID: 19005312 [TBL] [Abstract][Full Text] [Related]
12. Beyond informed consent. Bhutta ZA Bull World Health Organ; 2004 Oct; 82(10):771-7. PubMed ID: 15643799 [TBL] [Abstract][Full Text] [Related]
13. 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; Therapie; 2007; 62(3):193-7, 199-202. PubMed ID: 17803885 [TBL] [Abstract][Full Text] [Related]
14. Impact of French 'Comités de Protection des Personnes' on the readability of informed consent documents (ICD) in biomedical research: more information, but not better information. Paris A; Cracowski JL; Maison P; Radauceanu A; Cornu C; Hommel M Fundam Clin Pharmacol; 2005 Jun; 19(3):395-9. PubMed ID: 15910664 [TBL] [Abstract][Full Text] [Related]
15. [Consent: between legality and legitimacy or between "formal" and "informed" consent]. Lachaux B; Morasz L; Crison-Curinier J Encephale; 1998; 24(6):503-16. PubMed ID: 9949933 [TBL] [Abstract][Full Text] [Related]
16. [Legal regulations to protect under-aged donors issued by E.U. Member Countries. Analysis of the present situation and proposals]. Massimo L; Manfredini L Minerva Pediatr; 2001 Feb; 53(1):55-60. PubMed ID: 11309544 [TBL] [Abstract][Full Text] [Related]
17. Informed consent in medical research. Doctors are arrogant to think they need to debate issue of patient consent. Bratt DE BMJ; 1997 May; 314(7092):1477. PubMed ID: 9167569 [No Abstract] [Full Text] [Related]
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19. Data storage and DNA banking for biomedical research: informed consent, confidentiality, quality issues, ownership, return of benefits. A professional perspective. Godard B; Schmidtke J; Cassiman JJ; Aymé S Eur J Hum Genet; 2003 Dec; 11 Suppl 2():S88-122. PubMed ID: 14718939 [TBL] [Abstract][Full Text] [Related]
20. Science in Japan. Paper retraction puts focus on informed consent rules. Normile D Science; 2008 Jul; 321(5888):474. PubMed ID: 18653852 [No Abstract] [Full Text] [Related] [Next] [New Search]