{"data":{"id":"us-ky/krs-315.036","jurisdiction":"us-ky","citation":"KRS 315.036","heading":"Permit to be acquired by manufacturer -- Fee -- Records required --","body":"Report -- Exception.\n(1) Except as provided in subsection (4) of this section, each manufacturer of drugs\nshall be required to register with and obtain a permit from the board. Such p ermit\nshall be issued in accordance with policy and procedure prescribed by regulations of\nthe board. Each application shall be accompanied by a reasonable permit fee to be\nset by administrative regulation of the board, not to exceed two hundred fifty dollars\n($250) annually or increase more than twenty-five dollars ($25) per year.\n(2) Manufacturers shall be required to maintain accurate records of all drugs\nmanufactured, received and sold, as established by administrative regulation of the\nboard. Such records shall be made available to agents of the board for inspection at\nreasonable times. The board may require by regulation that manufacturers\nperiodically report to the board all drugs manufactured, received, and sold.\n(3) Failure to report to the board or  willful submission of inaccurate information shall\nbe grounds for disciplinary action under the provisions of KRS 315.131.\n(4) The provisions of subsection (1) of this section do not apply to a pharmacist who, in\nthe normal course of professional practice , compounds reasonable quantities of\ndrugs pursuant to or in anticipation of a valid prescription drug order.","path":["KRS Chapter 315"],"source_url":"https://apps.legislature.ky.gov/law/statutes/statute.aspx?id=30994","current_through":"Includes enactments through the 2026 Regular Session","vintage":"09/05/2026","retrieved_at":"2026-09-05T20:58:11Z","sha256":"e61be1ad8653045df7751ae54ba6a40742d96ab1bcf6bbf10222379adfcbf62c","source_id":"us-ky","stale":false,"prev":"us-ky/krs-315.0351","next":"us-ky/krs-315.038"},"notice":"GroundRules: Original legal text. Not legal advice."}