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