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CFR

423.150—Scope.

This subpart sets forth the requirements relating to the following:
(a) Drug utilization management programs, quality assurance measures and systems, and medication therapy management programs (MTMP) for Part D sponsors.
(b) Consumer satisfaction surveys of Part D plans.
(c) Electronic prescription drug programs for prescribers, dispensers, and Part D sponsors.
(d) Quality improvement organization (QIO) activities.
(e) Compliance deemed on the basis of accreditation.
(f) Accreditation organizations.
(g) Procedures for the approval of accreditation
organizations as a basis for deeming compliance.
[70 FR 4525, Jan. 28, 2005, as amended at 70 FR 67593, Nov. 7, 2005]
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