{"data":{"id":"us-ca/hsc-127691","jurisdiction":"us-ca","citation":"HSC § 127691","heading":"","body":"For purposes of this chapter, the following definitions apply:\n(a) “Generic drug” means a drug that is approved pursuant to subdivision (j) of Section 355 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. Sec. 301 et seq.), or a biosimilar, as defined under the federal Public Health Service Act (42 U.S.C. Sec. 262).\n(b) “Partnerships” include, but are not limited to, agreements for the procurement of generic prescription drugs by way of contracts, grant agreements, or purchasing by a payer, state governmental agency, group purchasing organization, nonprofit organization, or other entity.\n(c) “California Health and Human Services Agency” or “CHHSA” means the California Health and Human Services Agency, or any of its departments, including the Department of Health Care Access and Information, selected to implement this chapter.","path":["Health and Safety Code - HSC","DIVISION 107. HEALTH CARE ACCESS AND INFORMATION [127000. - 130079.]","PART 2. HEALTH POLICY AND PLANNING [127280. - 127774.]","CHAPTER 10. California Affordable Drug Manufacturing Act of 2020 [127690. - 127697.]"],"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":"b67ca48b09318cd3c98ca2b93c26efc2962d18561d028b298a9529ad23658a9a","source_id":"us-ca","stale":false,"prev":"us-ca/hsc-127690","next":"us-ca/hsc-127692"},"notice":"GroundRules: Original legal text. Not legal advice."}