Conn. Agencies Regs. § 17a-20-36

Current through December 4, 2024

Section 17a-20-36 - Informed consent for research, experimentation, or clinical trials

Policies shall be in place to protect the rights of children and their families during any research, experimentation, or clinical trials with signed informed consent including:

(1) A description of benefits to be expected;

(2) A description of the potential discomforts and risks;

(3) A description of alternative, non-experimental services that might also prove advantageous to them;

(4) A full explanation of the procedures to be followed, especially those that are experimental in nature;

(5) Assurance of their right to refuse to participate in any research project without comprising their access to services.

Conn. Agencies Regs. § 17a-20-36

Adopted effective February 1, 1999