Taking informed consent from patients/research participants asserts that:
A. Personal information will be freely available on all resources
B. Once the consent is given, the subjects cannot take it back
C. Intricate details need not be given about the procedure to participants
D. In some cases participants assent is taken to identify them with some specific traits (e.g., gender or organisation)
E. A standard treatment for a disease/injury may be denied to participants
Choose the correct answer from the options given below: