{"data":{"id":"us-ca/hsc-121310","jurisdiction":"us-ca","citation":"HSC § 121310","heading":"","body":"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.\n(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.\n(b) A copy of the informed consent shall be maintained with the woman’s medical records.","path":["Health and Safety Code - HSC","DIVISION 105. COMMUNICABLE DISEASE PREVENTION AND CONTROL [120100. - 122476.]","PART 4. HUMAN IMMUNODEFICIENCY VIRUS (HIV) [120775. - 121349.3.]","CHAPTER 14. Acquired Immune Deficiency Syndrome (AIDS) Clinical Trial Grant Award for the Prevention of Maternal Transmission of Human Immunodeficiency Virus (HIV) Infection [121300. - 121335.]"],"source_url":"https://downloads.leginfo.legislature.ca.gov/pubinfo_2025.zip","current_through":"2026-09-13","vintage":"","retrieved_at":"2026-09-14T05:56:33Z","sha256":"cd2d8d878ee29a1beec88618056ce9fe20af38dbe7362a93e7812aa638bb4165","source_id":"us-ca","stale":false,"prev":"us-ca/hsc-121305","next":"us-ca/hsc-121315"},"notice":"GroundRules: Original legal text. Not legal advice."}