Browsing Contribucions a congressos by Subject "61"

Now showing items 1-18 of 18

A Risk-based Approach to Patient Information?

Klingmann, Ingrid (2012-10-15)
Actituds i valors en medicina: debat

Abel i Fabre, Francesc (1996)
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)
Current practice of information for patients in Spain: Why do we need to reconsider the present informed consent process?

Hereu, Pilar (2012-10-15)
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)
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)