Answer for the Case
1. It is unethical, because the investigator has tell full
information not only to observe the effect of drug i.e he has to
explain clearly adveres event that may happen during the
study.Study participant has the right to access full information
2. A,Yes because taking much emphasis on benefit only rather
than the risk it may be called undue inducecment
B, Offering research subjects incentives for their
participation is a common practice that boosts recruitment but
also raises ethical concerns, such as undue inducement,
exploitation, and biased enrollment.
Answer for Case….
• 3. I do not think, because signing on the behalf of other
particpant with out having legal permission is unethical that
means violating respect for person, in addition clinical trial
should need written form of informed consent
• 4. Consent and community engagement (CE) in health research
are two aspects of a single concern—that research is carried out
in a respectful manner where social value is maximized.
• There are important overlaps and interdependencies between
consent and CE; for example, CE can provide insights into how
best to tailor consent to context and can be an important
component of consent processes.
Answer for Case….
• Engaging communities can also have intrinsic and
instrumental value beyond consent; for example, as a means of
showing respect and identifying appropriate ways of working
respectfully.
• In this paper we critically examine how CE and consent
processes are characterized, conducted, and evaluated in
diverse health research contexts, and propose a preliminary
research agenda to support future learning in these critical
areas