What is Informed Consent and Why is it Important?

Informed consent means that a person agrees to join a clinical trial after learning everything they need to know about it.

Before joining, participants are given:

  • A written document explaining the trial
  • Time to ask questions
  • A clear explanation of risks, benefits, and rights

No one can be forced to join a trial. Consent is completely voluntary, and participants can change their minds at any time. Informed consent is a basic ethical requirement in all research.

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