Contribucions a congressos

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)

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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

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 ﻿

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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