11/08/2023
What is Informed Consent?🤔
In clinical research, informed consent is a process through which individuals are provided with comprehensive and clear information about a clinical trial, including its purpose, potential risks and benefits, procedures, and alternatives, prior to voluntarily agreeing to participate. This process is designed to ensure that prospective research subjects fully understand the implications of their involvement and can make a well-informed decision regarding their participation.
In essence, informed consent is essential in upholding the ethical standards of research while respecting the autonomy and dignity of individuals who choose to participate. This practice is not only a legal requirement but also a moral imperative, and is crucial for the advancement of medical knowledge and the protection of the rights and welfare of research participants.