§ 121310

Added by Stats. 1995, Ch. 415, Sec. 7. Effective January 1, 1996.

A manufacturer, research institution, or researcher shall, prior to the administration of an AIDS vaccine to a research subject, obtain that woman’s informed consent, that shall comply with all applicable statutes and regulations.

(a)The informed consent shall contain a statement that significant new findings developed during the course of the research that may relate to the subject’s willingness to continue participation will be provided to the subject.
(b)A copy of the informed consent shall be maintained with the woman’s medical records.

Other sections in Chapter 14 - Acquired Immune Deficiency Syndrome (AIDS) Clinical Trial Grant Award for the Prevention of Maternal Transmission of Human Immunodeficiency Virus (HIV) Infection

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