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§ 423.150 Scope.
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.
42 C.F.R. § 423.150
Scope.
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Source: 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
Table of Contents
Subpart D—Cost Control and Quality Improvement Requirements
- §423.150 Scope.
- §423.153 Drug utilization management, quality assurance, medication therapy management programs (MTMPs), drug management programs, and access to Medicare Parts A and B claims data extracts.
- §423.154 Appropriate dispensing of prescription drugs in long-term care facilities under PDPs and MA-PD plans.
- §423.156 Consumer satisfaction surveys.
- §423.159 Electronic prescription drug program.
- §423.160 Standards for electronic prescribing.
- §423.162 Quality improvement organization activities.
- §423.165 Compliance deemed on the basis of accreditation.
- §423.168 Accreditation organizations.
- §423.171 Procedures for approval of accreditation as a basis for deeming compliance.
- §423.180 Basis and scope of the Part D Prescription Drug Plan Quality Rating System.
- §423.182 Part D Prescription Drug Plan Quality Rating System.
- §423.184 Adding, updating, and removing measures.
- §423.186 Calculation of Star Ratings.