{"data":{"id":"us/42-cfr-423.150","jurisdiction":"us","citation":"42 CFR 423.150","heading":"Scope.","body":"This subpart sets forth the requirements relating to the following:\n(a) Drug utilization management programs, quality assurance measures and systems, and MTM programs for Part D sponsors.\n(b) Appropriate dispensing of prescription drugs in long-term care facilities under PDPs and MA-PD plans.\n(c) Consumer satisfaction surveys of Part D plans.\n(d) Electronic prescription drug programs for prescribers, dispensers, and Part D sponsors.\n(e) Quality improvement organization (QIO) activities.\n(f) Compliance deemed on the basis of accreditation.\n(g) Accreditation organizations.\n(h) Procedures for the approval of accreditation organizations as a basis for deeming compliance.","path":["Title 42—Public Health","CHAPTER IV—CENTERS FOR MEDICARE \u0026 MEDICAID SERVICES, DEPARTMENT OF HEALTH AND HUMAN SERVICES","SUBCHAPTER B—MEDICARE PROGRAM","PART 423—VOLUNTARY MEDICARE PRESCRIPTION DRUG BENEFIT","Subpart D—Cost Control and Quality Improvement Requirements"],"source_url":"https://www.ecfr.gov/api/versioner/v1/full/2026-08-25/title-42.xml","current_through":"2026-08-25","vintage":"","retrieved_at":"2026-08-27T02:26:11Z","sha256":"83606a6209b103b660018c128a3529ab4d40672b8b6f127aebee62d67305ec31","source_id":"us-cfr","stale":true,"prev":"us/42-cfr-423.137","next":"us/42-cfr-423.153"},"notice":"GroundRules: Original legal text. Not legal advice."}