Requirements; notice

410 ILCS 416/20, under Clinical Trial Participation Program Act.

410 ILCS 416/20

(410 ILCS 416/20)

    Sec. 20. Requirements; notice.     (a) The program:         (1) must collaborate with physicians, health care     providers, and clinical trial sponsors to notify a prospective subject about the program when:            (A) the prospective subject consents to a         clinical trial; or            (B) funding is available to provide the program         for the clinical trial in which the prospective subject participates;        (2) must reimburse subjects based on financial need,     which may include reimbursement to subjects whose income is at or below 700% of the federal poverty level;        (3) must provide reimbursement for ancillary costs,     including costs described under Section 15, to eliminate the financial barriers to enrollment in a clinical trial;        (4) may provide reimbursement for reasonable     ancillary costs, including costs described under Section 15, to one family member, friend, or other person who attends a clinical trial to support a subject; and        (5) must comply with applicable federal and State     laws.    (b) The independent third-party organization administering the program shall provide written notice to prospective subjects of the requirements described under subsection (a).

(Source: P.A. 103-227, eff. 6-30-23.)