Cristina Ferrer‐Albero
Biographic Data
| ID | 8983183 |
|---|---|
| NAME | Cristina Ferrer‐Albero |
| GIVEN NAMES | Cristina |
| FAMILY NAME | Ferrer‐Albero |
| SIGNATURE | ALBERO C F |
| AFFILIATIONS | Facultad de Medicina y Ciencias de la Salud Universidad Católica de Valencia San Vicente Mártir Valencia Spain |
| ORCID | 0000-0001-8904-0532 |
| VERIFIED | Yes |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2022 |
| LATEST PUBLICATION YEAR | 2023 |
| H-INDEX | 0 |
Co‐creation of information materials within the assent process
INTRODUCTION: The informed consent process is key to safeguarding the autonomy of the participant in medical research. For this process to be valid, the information presented to the potential participant should meet their needs and be understood by them. The i-CONSENT project has developed 'Guidelines for adapting the informed consent process in clinical trials' which aim to improve informed consent so that they are easier to understand and bette…
Keys to improving the informed consent process in research
The ethical and legal governance of all aspects of informed consent in research is becoming increasingly extensive and complex. Instead of a single directive, informed consent is governed by a series of international rules applied to biomedical research, clinical trials and biobanks, while various ethical guidelines for research have been published by different international bodies. Informed consent is an essential part of any research involving …
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Keys to improving the informed consent process in research
The ethical and legal governance of all aspects of informed consent in research is becoming increasingly extensive and complex. Instead of a single directive, informed consent is governed by a series of international rules applied to biomedical research, clinical trials and biobanks, while various ethical guidelines for research have been published by different international bodies. Informed consent is an essential part of any research involving …
Co‐creation of information materials within the assent process
INTRODUCTION: The informed consent process is key to safeguarding the autonomy of the participant in medical research. For this process to be valid, the information presented to the potential participant should meet their needs and be understood by them. The i-CONSENT project has developed 'Guidelines for adapting the informed consent process in clinical trials' which aim to improve informed consent so that they are easier to understand and bette…
Alternative medicine (2 works) · Computer Science (2 works) · Ethics in Clinical Research (2 works) · Family medicine (2 works) · Informed consent (2 works) · Medical education (2 works) · Medicine (2 works) · Psychology (2 works) · Autonomy (1 work) · Biobank (1 work)