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Notes

§423.150. Scope.

42 C.F.R. § 423.150

This subpart sets forth the requirements relating to the following:
(a)
Drug utilization management programs, quality assurance measures and systems, and MTM programs for Part D sponsors.
(b)
Appropriate dispensing of prescription drugs in long-term care facilities under PDPs and MA-PD plans.
(c)
Consumer satisfaction surveys of Part D plans.
(d)
Electronic prescription drug programs for prescribers, dispensers, and Part D sponsors.
(e)
Quality improvement organization (QIO) activities.
(f)
Compliance deemed on the basis of accreditation.
(g)
Accreditation organizations.
(h)
Procedures for the approval of accreditation organizations as a basis for deeming compliance.
Notes, amendments, and revision history

Amendments

[70 FR 4525, Jan. 28, 2005, as amended at 70 FR 67593, Nov. 7, 2005; 76 FR 21573, Apr. 15, 2011; 89 FR 30834, Apr. 23, 2024]

Authority

Authority: 42 U.S.C. 1302, 1306, 1395w-101 through 1395w-152, and 1395hh.

Source

Source: 70 FR 4525, Jan. 28, 2005, unless otherwise noted.

Amendments

[70 FR 4525, Jan. 28, 2005, as amended at 70 FR 67593, Nov. 7, 2005; 76 FR 21573, Apr. 15, 2011; 89 FR 30834, Apr. 23, 2024]