Objective: To identify and highlight challenges related to informed consent process for clinical trials in sub-Saharan Africa. Data sources: Published original research findings and reviews in the English literature, together with anecdotal information from our current professional experiences with clinical trials. Design: Review of peer-reviewed articles. Data extraction: Online searches were done and requests for reprints from corresponding authors and institutional subscription. Data synthesis: Information categorised accordingly.Results: Informed consent for clinical trials conducted in sub-Saharan Africa (SSA) is not always “truly informed” or “truly voluntary”. Guidelines for obtaining informed consent are often difficult to implement...
Introduction.Guidelines for biomedical research involving human subjects require that research shoul...
To explore the advantages and challenges of working with the Good Clinical Practice (GCP)-Internatio...
This study was designed to evaluate the quality of informed consent practiced by healthcare profess...
Objective: To identify and highlight challenges related to informed consent processfor clinical tria...
Regulations are vague regarding the appropriate decision-maker and authority to consent for children...
BACKGROUND:Informed consent is an ethical and legal requirement for research involving human partici...
Objectives: To identify possible existence of therapeutic misconception and its effects on clinical ...
OBJECTIVE: Previous reviews on participants' comprehension of informed consent information have focu...
Gaurav Puppalwar, Meenakshi Mourya, Ganesh Kadhe, Amey Mane Medical Affairs, Wockhardt Limited, Wock...
The regulatory guidelines on obtaining informed consent require that all protocols be reviewed by an...
African institutions that perform health research need to continuously evaluate their practices in o...
A study was conducted among participants in an antiretroviral therapy (ART) clinical trial to determ...
Background/rationale: Ethical issues regarding HIV/AIDS human research in the developing world remai...
Introduction: In settings with low literacy levels ensuring that participants are fully-informed bef...
Introduction: Informed consent is a critical issue especially in conducting clinical trials that exp...
Introduction.Guidelines for biomedical research involving human subjects require that research shoul...
To explore the advantages and challenges of working with the Good Clinical Practice (GCP)-Internatio...
This study was designed to evaluate the quality of informed consent practiced by healthcare profess...
Objective: To identify and highlight challenges related to informed consent processfor clinical tria...
Regulations are vague regarding the appropriate decision-maker and authority to consent for children...
BACKGROUND:Informed consent is an ethical and legal requirement for research involving human partici...
Objectives: To identify possible existence of therapeutic misconception and its effects on clinical ...
OBJECTIVE: Previous reviews on participants' comprehension of informed consent information have focu...
Gaurav Puppalwar, Meenakshi Mourya, Ganesh Kadhe, Amey Mane Medical Affairs, Wockhardt Limited, Wock...
The regulatory guidelines on obtaining informed consent require that all protocols be reviewed by an...
African institutions that perform health research need to continuously evaluate their practices in o...
A study was conducted among participants in an antiretroviral therapy (ART) clinical trial to determ...
Background/rationale: Ethical issues regarding HIV/AIDS human research in the developing world remai...
Introduction: In settings with low literacy levels ensuring that participants are fully-informed bef...
Introduction: Informed consent is a critical issue especially in conducting clinical trials that exp...
Introduction.Guidelines for biomedical research involving human subjects require that research shoul...
To explore the advantages and challenges of working with the Good Clinical Practice (GCP)-Internatio...
This study was designed to evaluate the quality of informed consent practiced by healthcare profess...