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Biomedical Research in Developing Countries - UNICRI

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Petr<strong>in</strong>i C. (Ed.), Informed consent to treatment of persons with dementia: ethical,<br />

deontological, juridical aspects, Rapporto ICTISAN 08/03, 2008<br />

Petros B., <strong>Biomedical</strong> <strong>Research</strong> and Ethics <strong>in</strong> Ethiopia, A Keynote Address, (date unknown)<br />

Pharmaceutical <strong>Research</strong> and Manufacturers of America, PhRMA Annual Membership<br />

Survey, 2006<br />

Pich J. et al., Role of a <strong>Research</strong> Ethics Committee <strong>in</strong> follow up and publication of results,<br />

The Lancet, 2003, Vol. 361, No. 9376, Page 2246<br />

PIC/S – Pharmaceutical Inspection Convention Co-operation Scheme, Press release:<br />

PIC/S Committee Meet<strong>in</strong>g, Geneva, Switzerland 23 May 2007<br />

Positifs, 2007, Anno XVI, No. 81-82<br />

Ponc<strong>in</strong> J., Des essais cl<strong>in</strong>iques dans les pays du Sud? Oui, mais…, IRCM Centre de<br />

Bioéthique, L’Observatoire de la Génétique, No. 7, 2002<br />

Public Health Fact Sheet, Barriers to Access: Medication-Assisted Treatment and Injection-<br />

Driven HIV Epidemics, 2008, No. 4<br />

Rachier A., Legislative and adm<strong>in</strong>istrative measures for the implementation of the<br />

Universal Declaration on Bioethics and Human Rights <strong>in</strong> Africa, (date unknown)<br />

Ramahi I., Silverman H., Cl<strong>in</strong>ical <strong>Research</strong> Law <strong>in</strong> Jordan: an Ethical Analysis,<br />

Develop<strong>in</strong>g World Bioethics, 12 December 2007<br />

Ramasubbu K., Gurm H., Litaker D., Gender Bias <strong>in</strong> Cl<strong>in</strong>ical Trials: Do Double Standards<br />

Still Apply?, Journal Of Women’s Health & Gender-Based Medic<strong>in</strong>e, 2001, Vol. 10, No.<br />

8, Pages 757-764<br />

Ramsay S., African health researchers unite, The Lancet, 2002, Vol. 360, No. 9346,<br />

Pages 1665-1666<br />

Rehnquist J., Cl<strong>in</strong>ical Trial Web Site, A Promis<strong>in</strong>g Tool To Foster Informed Consent, US<br />

Department of Health and Human Services, Office of Inspector General, 2002<br />

Rehnquist J., The Globalization of Cl<strong>in</strong>ical Trials, A Grow<strong>in</strong>g Challenge <strong>in</strong> Protect<strong>in</strong>g<br />

Human Subjects, US Department of Health and Human Services, Office of Inspector<br />

General, 2001<br />

Repubblica Italiana, Decreto Legislativo n. 211 del 24 Giugno 2003, Attuazione della<br />

direttiva 2001/20/CE relativa all’applicazione della buona pratica cl<strong>in</strong>ica nell’esecuzione<br />

delle sperimentazioni cl<strong>in</strong>iche di medic<strong>in</strong>ali per uso cl<strong>in</strong>ico, Gazzetta Ufficiale n. 184 del<br />

9 Agosto 2003<br />

Repubblica Italiana, Decreto Legislativo n. 200 del 6 novembre 2007, Attuazione della<br />

direttiva 2005/28/CE recante pr<strong>in</strong>cipi e l<strong>in</strong>ee guida dettagliate per la buona pratica cl<strong>in</strong>ica<br />

relativa ai medic<strong>in</strong>ali <strong>in</strong> fase di sperimentazione a uso umano, nonché requisiti per<br />

l'autorizzazione alla fabbricazione o importazione di tali medic<strong>in</strong>ali, Gazzetta Ufficiale n.<br />

261 del 09 Novembre 2007<br />

232

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