Contribucions a congressos

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El dret del pacient a la informació i a disposar d'ell mateix

Abel i Fabre, Francesc (1996)
Actituds i valors en medicina: debat

Abel i Fabre, Francesc (1996)
Enginyeria genètica i bioètica. Resposta a tres preguntes

Abel i Fabre, Francesc (1996)
Autonomia i voluntats anticipades

Terribas i Sala, Núria (2013-02-12)
Experiences with National Differences in Information Package Constitution

Mehrer, Heike; Dodsworth, Nicky (2012-10-15)
A Risk-based Approach to Patient Information?

Klingmann, Ingrid (2012-10-15)
How Can Technology Improve the IC Process?

Mascalzoni, Deborah (2012-10-15)
Can we ease the ethical review of Clinical Trials in the EU? (within current/ future law)

Herrero-Martínez, Estebán (2012-10-15)
El proceso de revisión ética en España y en los ensayos multinacionales

Hernández, César (2012-10-15)
The European Commission’s Regulation Proposal

Klingmann, Ingrid (2012-10-15)
Approaches to Informed Consent in Clinical Trials With Unconscious Patients

Iwanowski, Piotr (2012-10-15)
¿Cómo afectará esta propuesta a los ensayos clínicos en España?

Avendaño Sola, Cristina (2005-10-15)
Clinical Trials in Emergencies: When consent might kill you

Haleema, Shakur (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)
Current practice of information for patients in Spain: Why do we need to reconsider the present informed consent process?

Hereu, Pilar (2012-10-15)
Process adaptation of consent to the needs of the patients

Moreno, Coloma (2012-10-15)
Guidance on What makes a good Participant Information Sheet? Participant Information Sheets (PtIS) and Consent

Davies, Hugh (2012-10-15)
What do patients want and need to know when participating in clinical trials?

Hasurdjiev, Stanimir (2012-10-01)
Optimitzation of Informed Consent in Paediatric trials

Cusí Sánchez, Victòria (2012-10-15)

Contribucions a congressos

Browse by

Recent Submissions

El dret del pacient a la informació i a disposar d'ell mateix ﻿

Actituds i valors en medicina: debat ﻿

Enginyeria genètica i bioètica. Resposta a tres preguntes ﻿

Autonomia i voluntats anticipades ﻿

Experiences with National Differences in Information Package Constitution ﻿

A Risk-based Approach to Patient Information? ﻿

How Can Technology Improve the IC Process? ﻿

Can we ease the ethical review of Clinical Trials in the EU? (within current/ future law) ﻿

El proceso de revisión ética en España y en los ensayos multinacionales ﻿

The European Commission’s Regulation Proposal ﻿

Approaches to Informed Consent in Clinical Trials With Unconscious Patients ﻿

¿Cómo afectará esta propuesta a los ensayos clínicos en España? ﻿

Clinical Trials in Emergencies: When consent might kill you ﻿

Proposal for a Regulation of the European Parliament and of the Council ﻿

The EFGCP Initiative on Patient Information Sheet (PIS) Improvement ﻿

Current practice of information for patients in Spain: Why do we need to reconsider the present informed consent process? ﻿

Process adaptation of consent to the needs of the patients ﻿

Guidance on What makes a good Participant Information Sheet? Participant Information Sheets (PtIS) and Consent ﻿

What do patients want and need to know when participating in clinical trials? ﻿

Optimitzation of Informed Consent in Paediatric trials ﻿

El dret del pacient a la informació i a disposar d'ell mateix

Actituds i valors en medicina: debat

Enginyeria genètica i bioètica. Resposta a tres preguntes

Autonomia i voluntats anticipades

Experiences with National Differences in Information Package Constitution

A Risk-based Approach to Patient Information?

How Can Technology Improve the IC Process?

Can we ease the ethical review of Clinical Trials in the EU? (within current/ future law)

El proceso de revisión ética en España y en los ensayos multinacionales

The European Commission’s Regulation Proposal

Approaches to Informed Consent in Clinical Trials With Unconscious Patients

¿Cómo afectará esta propuesta a los ensayos clínicos en España?

Clinical Trials in Emergencies: When consent might kill you

Proposal for a Regulation of the European Parliament and of the Council

The EFGCP Initiative on Patient Information Sheet (PIS) Improvement

Current practice of information for patients in Spain: Why do we need to reconsider the present informed consent process?

Process adaptation of consent to the needs of the patients

Guidance on What makes a good Participant Information Sheet? Participant Information Sheets (PtIS) and Consent

What do patients want and need to know when participating in clinical trials?

Optimitzation of Informed Consent in Paediatric trials