Visualitzant Contribucions a congressos per autor/a "Universitat Ramon Llull. Institut Borja de Bioètica"
Ara mostrant els elements 1-20 de 20
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A Risk-based Approach to Patient Information?
Klingmann, Ingrid (2012-10-15) -
Actituds i valors en medicina: debat
Abel i Fabre, Francesc (1996) -
Approaches to Informed Consent in Clinical Trials With Unconscious Patients
Iwanowski, Piotr (2012-10-15) -
Autonomia i voluntats anticipades
Terribas i Sala, Núria (2013-02-12) -
Can we ease the ethical review of Clinical Trials in the EU? (within current/ future law)
Herrero-Martínez, Estebán (2012-10-15) -
Clinical Trials in Emergencies: When consent might kill you
Haleema, Shakur (2012-10-15) -
¿Cómo afectará esta propuesta a los ensayos clínicos en España?
Avendaño Sola, Cristina (2005-10-15) -
El dret del pacient a la informació i a disposar d'ell mateix
Abel i Fabre, Francesc (1996) -
El proceso de revisión ética en España y en los ensayos multinacionales
Hernández, César (2012-10-15) -
Enginyeria genètica i bioètica. Resposta a tres preguntes
Abel i Fabre, Francesc (1996) -
Experiences with National Differences in Information Package Constitution
Mehrer, Heike; Dodsworth, Nicky (2012-10-15) -
Guidance on What makes a good Participant Information Sheet? Participant Information Sheets (PtIS) and Consent
Davies, Hugh (2012-10-15) -
How Can Technology Improve the IC Process?
Mascalzoni, Deborah (2012-10-15) -
Optimitzation of Informed Consent in Paediatric trials
Cusí Sánchez, Victòria (2012-10-15) -
Process adaptation of consent to the needs of the patients
Moreno, Coloma (2012-10-15) -
Proposal for a Regulation of the European Parliament and of the Council
Ernst, Singer (2012-10-15) -
The EFGCP Initiative on Patient Information Sheet (PIS) Improvement
Gerhard, Fortwengel (2012-10-15) -
The European Commission’s Regulation Proposal
Klingmann, Ingrid (2012-10-15) -
What do patients want and need to know when participating in clinical trials?
Hasurdjiev, Stanimir (2012-10-01)