Cargando…
Informed consent: Issues and challenges
Informed consent is an ethical and legal requirement for research involving human participants. It is the process where a participant is informed about all aspects of the trial, which are important for the participant to make a decision and after studying all aspects of the trial the participant vol...
Autores principales: | Nijhawan, Lokesh P., Janodia, Manthan D., Muddukrishna, B. S., Bhat, K. M., Bairy, K. L., Udupa, N., Musmade, Prashant B. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3777303/ https://www.ncbi.nlm.nih.gov/pubmed/24083200 http://dx.doi.org/10.4103/2231-4040.116779 |
Ejemplares similares
-
Development and Validation of Liquid Chromatographic Method for Estimation of Naringin in Nanoformulation
por: Musmade, Kranti P., et al.
Publicado: (2014) -
Medical device vigilance systems: India, US, UK, and Australia
por: Gupta, Pooja, et al.
Publicado: (2010) -
Regulatory Aspects of Pharmaceuticals’ Exports in Gulf Cooperation Council Countries
por: Pateriya, S, et al.
Publicado: (2011) -
Development of a sustainable access to medicine model in the Caribbean: a case study of the chronic disease assistance program
por: Maharaj, Sandeep, et al.
Publicado: (2014) -
Informed Consent in Biomedical Research: Scopes and Challenges
por: Chatterjee, Kingshuk, et al.
Publicado: (2021)