StacksVerified U.S. regulatory reference

42 CFR §423.150

Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov ↗
This subpart sets forth the requirements relating to the following:
  1. (a)Drug utilization management programs, quality assurance measures and systems, and MTM programs for Part D sponsors.
  2. (b)Appropriate dispensing of prescription drugs in long-term care facilities under PDPs and MA-PD plans.
  3. (c)Consumer satisfaction surveys of Part D plans.
  4. (d)Electronic prescription drug programs for prescribers, dispensers, and Part D sponsors.
  5. (e)Quality improvement organization (QIO) activities.
  6. (f)Compliance deemed on the basis of accreditation.
  7. (g)Accreditation organizations.
  8. (h)Procedures for the approval of accreditation organizations as a basis for deeming compliance.